Canonical Allele Identifier: PA148589
Gene: ATP6V0A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036595.2:p.Lys374Arg
CA148588
NM_012463.4:c.1121A>G