Allele Registry

Canonical Allele Identifier: PA916003081

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV002518408

RCV003463693

ClinVar Variation:

242582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Trp298Cys	CA052835 NM_001199291.3:c.894G>T CA360867312 NM_001199291.3:c.894G>C