Allele Registry

Canonical Allele Identifier: PA105401

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000023152

RCV002513181

RCV003330398

ClinVar Variation:

30228

HGVS (amino-acid)	Matching Registered Transcripts
NP_000405.1:p.Tyr217Cys	CA129040 NM_000414.4:c.650A>G