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: | ACP1 |
| Type: | single nucleotide variant |
| Location: |
Chr2: 272223
- assembly
GRCh38 Chr2: 272223 - assembly GRCh37 |
| References: | dbSNP:
886043643 |
Condition |
|
| Disease: | not provided |