Allele Registry

Canonical Allele Identifier: PA2828525165

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV002580362

ClinVar Variation:

1902544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361428.1:p.Arg139Leu	CA360867151 NM_001374499.1:c.416G>T