Canonical Allele Identifier: PA105650
Gene: HSD17B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 4877
ClinVar RCV Id: RCV000005153 RCV000514552 RCV000584139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000188.1:p.Arg80Trp
CA117114
NM_000197.2:c.238C>T