GENETIC ENCYCLOPEDIA
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NM_004300.4(ACP1):c.231+73G>A AND not provided

Significance: Uncertain significance
ClinVar: RCV000351394

Variant: NM_004300.4(ACP1):c.231+73G>A

Type: Variant
Allele: NM_004300.4(ACP1):c.231+73G>A 271700
Gene:
Type: single nucleotide variant
Location: Chr2: 272223 - assembly GRCh38
Chr2: 272223 - assembly GRCh37
References: dbSNP: 886043643

Condition

Disease: not provided