Canonical Allele Identifier: PA357899
Gene: ATP6V1A HGNC NCBI

Linked Data

ClinVar Variation Id: 224820
ClinVar RCV Id: RCV000210381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001681.2:p.Asn314Asp
CA357898
NM_001690.4:c.940A>G