Allele Registry

Canonical Allele Identifier: PA2826819075

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000125467

RCV000675096

ClinVar Variation:

137618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Pro489Leu	CA163185 NM_001292027.2:c.1466C>T