Canonical Allele Identifier: PA2573164410
Gene: HSD17B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449786
ClinVar RCV Id: RCV001989806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000188.1:p.Ala275Val
CA5140246
NM_000197.2:c.824C>T