Canonical Allele Identifier: PA2829300493
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_001387266.1:p.Ala174Val
CA263810239
NM_001400337.1:c.521C>T