Canonical Allele Identifier: PA2828526738
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1202909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361432.1:p.Met68Thr
CA3381892
NM_001374503.1:c.203T>C