Canonical Allele Identifier: PA2826239803
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1202909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Met230Thr
CA3381892
NM_001199291.3:c.689T>C