Allele Registry

Canonical Allele Identifier: PA2826240425

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000125467

RCV000675096

ClinVar Variation:

137618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186221.1:p.Pro495Leu	CA163185 NM_001199292.2:c.1484C>T