Canonical Allele Identifier: PA2828526735
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_001361432.1:p.Arg62Trp
CA3381885
NM_001374503.1:c.184C>T