Allele Registry

Canonical Allele Identifier: PA2826240200

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV001937673

ClinVar Variation:

1406932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186221.1:p.Arg230Gly	CA360867149 NM_001199292.2:c.688C>G