Allele Registry

Canonical Allele Identifier: PA052869

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV002518408

RCV003463693

ClinVar Variation:

242582

HGVS (amino-acid)	Matching Registered Transcripts
NP_000405.1:p.Trp273Cys	CA052835 NM_000414.4:c.819G>T CA360867312 NM_000414.4:c.819G>C