Allele Registry

Canonical Allele Identifier: PA916018615

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000732613

ClinVar Variation:

596699

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278957.1:p.Tyr77Phe	CA360866924 NM_001292028.2:c.230A>T