Allele Registry

Canonical Allele Identifier: PA2826819354

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV002518408

RCV003463693

ClinVar Variation:

242582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278957.1:p.Trp133Cys	CA052835 NM_001292028.2:c.399G>T CA360867312 NM_001292028.2:c.399G>C