Allele Registry

Canonical Allele Identifier: PA2573187448

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV001937673

ClinVar Variation:

1406932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Arg273Gly	CA360867149 NM_001199291.3:c.817C>G