Allele Registry

Canonical Allele Identifier: PA2826818822

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000023152

RCV002513181

RCV003330398

ClinVar Variation:

30228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Tyr193Cys	CA129040 NM_001292027.2:c.578A>G