Canonical Allele Identifier: PA658717994
Gene: HSD17B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 492766
ClinVar RCV Id: RCV000583085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000188.1:p.Pro193His
CA374123956
NM_000197.2:c.578C>A