Canonical Allele Identifier: PA658807721
Gene: VIPAS39 HGNC NCBI

Linked Data

ClinVar Variation Id: 498683
ClinVar RCV Id: RCV000594831 RCV000765181 RCV003915706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071350.2:p.Ser485Arg
CA7287709
NM_022067.4:c.1455C>A
CA390696012
NM_022067.4:c.1455C>G
CA390696017
NM_022067.4:c.1453A>C