Allele Registry

Canonical Allele Identifier: PA2826239740

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000008096

ClinVar Variation:

7657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Arg131Pro	CA118962 NM_001199291.3:c.392G>C