Canonical Allele Identifier: PA2828526718
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1941206
ClinVar RCV Id: RCV002643024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361432.1:p.Ser40Pro
CA360866260
NM_001374503.1:c.118T>C