Allele Registry

Canonical Allele Identifier: PA645496536

Gene: HSD17B4 HGNC NCBI

ClinVar Variation Id: 371607

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Pro26Leu	CA3381653 NM_001199291.3:c.77C>T