Allele Registry

Canonical Allele Identifier: PA105947

Gene: ATP6V0A4 HGNC NCBI

ClinVar RCV:

RCV000005461

RCV000244134

RCV001512758

RCV001807628

RCV002620552

ClinVar Variation:

5154

2188863

HGVS (amino-acid)	Matching Registered Transcripts
NP_065683.2:p.Met580Thr	CA117293 NM_020632.3:c.1739T>C CA2580077501 NM_020632.3:c.1739_1740delinsCA