Allele Registry

Canonical Allele Identifier: PA645496626

Gene: HSD17B4 HGNC NCBI

ClinVar Variation Id: 226666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Ser547Arg	CA3382309 NM_001199291.3:c.1641T>A CA360869162 NM_001199291.3:c.1639A>C CA360869167 NM_001199291.3:c.1641T>G