Allele Registry

Canonical Allele Identifier: PA916003065

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000409273

RCV000815715

RCV001840499

ClinVar Variation:

371366

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Arg273Cys	CA16040964 NM_001199291.3:c.817C>T