Canonical Allele Identifier: PA2826178065
Gene: VIPAS39 HGNC NCBI

Linked Data

ClinVar Variation Id: 2629356
ClinVar RCV Id: RCV003412159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180243.1:p.Ala254Val
CA263810239
NM_001193314.2:c.761C>T