Canonical Allele Identifier: PA2580108426
Gene: HSD17B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2482188
ClinVar RCV Id: RCV003214622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000188.1:p.Leu212Arg
CA374123580
NM_000197.2:c.635T>G