Allele Registry

Canonical Allele Identifier: PA916003205

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000125467

RCV000675096

ClinVar Variation:

137618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Pro538Leu	CA163185 NM_001199291.3:c.1613C>T