Allele Registry

Canonical Allele Identifier: PA236238

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000171385

RCV003317125

RCV003765072

RCV003987413

ClinVar Variation:

191199

HGVS (amino-acid)	Matching Registered Transcripts
NP_000405.1:p.Asn176Asp	CA236237 NM_000414.4:c.526A>G