Canonical Allele Identifier: PA645498549
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 350468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Arg543His
CA3382344
NM_000414.4:c.1628G>A