Allele Registry

Canonical Allele Identifier: PA2825164801

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV001937673

ClinVar Variation:

1406932

HGVS (amino-acid)	Matching Registered Transcripts
NP_000405.1:p.Arg248Gly	CA360867149 NM_000414.4:c.742C>G