Canonical Allele Identifier: PA645424098
Gene: ATP6V0A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432720
ClinVar RCV Id: RCV000498620 RCV002056828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036595.2:p.Met357Leu
CA6861832
NM_012463.4:c.1069A>T
CA387155364
NM_012463.4:c.1069A>C