Canonical Allele Identifier: PA2828525524
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2044553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361429.1:p.Arg52Trp
CA3381885
NM_001374500.1:c.154C>T