Allele Registry

Canonical Allele Identifier: PA2826240173

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000732613

ClinVar Variation:

596699

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186221.1:p.Tyr199Phe	CA360866924 NM_001199292.2:c.596A>T