Allele Registry

Canonical Allele Identifier: PA105371

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000008096

ClinVar Variation:

7657

HGVS (amino-acid)	Matching Registered Transcripts
NP_000405.1:p.Arg106Pro	CA118962 NM_000414.4:c.317G>C