Allele Registry

Canonical Allele Identifier: PA2826819553

Gene: HSD17B4 HGNC NCBI

ClinVar Allele:

141321

ClinVar RCV:

RCV000125467

RCV000675096

ClinVar Variation:

137618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278957.1:p.Pro373Leu	CA163185 NM_001292028.2:c.1118C>T