Canonical Allele Identifier: PA1139722819
Gene: ATP6V0A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 945705
ClinVar RCV Id: RCV001760196 RCV001216411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036595.2:p.Asn373Ser
CA6861849
NM_012463.4:c.1118A>G