Canonical Allele Identifier: PA2825164765
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2044553
ClinVar RCV Id: RCV002903774 RCV003317625 RCV003324053
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Arg199Trp
CA3381885
NM_000414.4:c.595C>T