Canonical Allele Identifier: PA2573090032
Gene: ATP6V0A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1307521
ClinVar RCV Id: RCV001760939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036595.2:p.Tyr452Ser
CA387157363
NM_012463.4:c.1355A>C