Allele Registry

Canonical Allele Identifier: PA2826239780

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000171385

RCV003317125

RCV003765072

RCV003987413

ClinVar Variation:

191199

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Asn201Asp	CA236237 NM_001199291.3:c.601A>G