Allele Registry

Canonical Allele Identifier: PA645498458

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000409273

RCV000815715

RCV001840499

ClinVar Variation:

371366

HGVS (amino-acid)	Matching Registered Transcripts
NP_000405.1:p.Arg248Cys	CA16040964 NM_000414.4:c.742C>T