Allele Registry

Canonical Allele Identifier: PA2826818850

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000409273

RCV000815715

RCV001840499

ClinVar Variation:

371366

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Arg224Cys	CA16040964 NM_001292027.2:c.670C>T