Allele Registry

Canonical Allele Identifier: PA163186

Gene: HSD17B4 HGNC NCBI

ClinVar Allele:

141321

ClinVar RCV:

RCV000125467

RCV000675096

ClinVar Variation:

137618

HGVS (amino-acid)	Matching Registered Transcripts
NP_000405.1:p.Pro513Leu	CA163185 NM_000414.4:c.1538C>T