Allele Registry

Canonical Allele Identifier: PA2826819082

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000125466

RCV000672665

RCV000825530

RCV001849905

RCV003144135

ClinVar Variation:

137617

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Ile492Thr	CA163183 NM_001292027.2:c.1475T>C