Allele Registry

Canonical Allele Identifier: PA916018614

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000023152

RCV002513181

RCV003330398

ClinVar Variation:

30228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278957.1:p.Tyr77Cys	CA129040 NM_001292028.2:c.230A>G