Allele Registry

Canonical Allele Identifier: PA2826240130

Gene: HSD17B4 HGNC NCBI

ClinVar Variation Id: 1713648

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186221.1:p.Tyr146Cys	CA360866180 NM_001199292.2:c.437A>G