Canonical Allele Identifier: PA1139680798
Gene: HSD17B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 913468
ClinVar RCV Id: RCV001167098 RCV003727930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000188.1:p.Glu214Gly
CA5140318
NM_000197.2:c.641A>G