Canonical Allele Identifier: PA2741812005
Gene: HSD17B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2674669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000188.1:p.Val225Met
CA196613902
NM_000197.2:c.673G>A