Allele Registry

Canonical Allele Identifier: PA2826240198

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV002580362

ClinVar Variation:

1902544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186221.1:p.Arg230Leu	CA360867151 NM_001199292.2:c.689G>T