Allele Registry

Canonical Allele Identifier: PA916018610

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000171385

RCV003317125

RCV003765072

RCV003987413

ClinVar Variation:

191199

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278957.1:p.Asn36Asp	CA236237 NM_001292028.2:c.106A>G