Canonical Allele Identifier: PA1139722838
Gene: ATP6V0A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 916153
ClinVar RCV Id: RCV001171666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036595.2:p.Gly389Arg
CA387155873
NM_012463.4:c.1165G>A
CA387155874
NM_012463.4:c.1165G>C