Allele Registry

Canonical Allele Identifier: PA2826240227

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV002518408

RCV003463693

ClinVar Variation:

242582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186221.1:p.Trp255Cys	CA052835 NM_001199292.2:c.765G>T CA360867312 NM_001199292.2:c.765G>C