Allele Registry

Canonical Allele Identifier: PA658663258

Gene: ATP6V0A2 HGNC NCBI

ClinVar Variation Id: 446885

HGVS (amino-acid)	Matching Registered Transcripts
NP_036595.2:p.Ala795Val	CA6862234 NM_012463.4:c.2384C>T