Allele Registry

Canonical Allele Identifier: PA2828525166

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV001937673

ClinVar Variation:

1406932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361428.1:p.Arg139Gly	CA360867149 NM_001374499.1:c.415C>G