Allele Registry

Canonical Allele Identifier: PA2826819109

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000125468

RCV000730879

RCV001849906

RCV003467098

ClinVar Variation:

137619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Arg519Pro	CA163187 NM_001292027.2:c.1556G>C