Allele Registry

Canonical Allele Identifier: PA105938

Gene: ATP6V0A4 HGNC NCBI

ClinVar RCV:

RCV001807625

RCV001851665

ClinVar Variation:

5151

HGVS (amino-acid)	Matching Registered Transcripts
NP_065683.2:p.Gly820Arg	CA117288 NM_020632.3:c.2458G>A CA369373931 NM_020632.3:c.2458G>C