Canonical Allele Identifier: PA2825164739
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332792
ClinVar RCV Id: RCV001806366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Tyr156His
CA360866121
NM_000414.4:c.466T>C