Canonical Allele Identifier: PA2828524199
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 198079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361426.1:p.Arg106His
CA203225
NM_001374497.1:c.317G>A