Allele Registry

Canonical Allele Identifier: PA916003347

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000008096

ClinVar Variation:

7657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186221.1:p.Arg88Pro	CA118962 NM_001199292.2:c.263G>C