Allele Registry

Canonical Allele Identifier: PA2828525353

Gene: HSD17B4 HGNC NCBI

ClinVar Variation Id: 226666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361428.1:p.Ser413Arg	CA3382309 NM_001374499.1:c.1239T>A CA360869162 NM_001374499.1:c.1237A>C CA360869167 NM_001374499.1:c.1239T>G