Allele Registry

Canonical Allele Identifier: PA913198307

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000732613

ClinVar Variation:

596699

HGVS (amino-acid)	Matching Registered Transcripts
NP_000405.1:p.Tyr217Phe	CA360866924 NM_000414.4:c.650A>T