Canonical Allele Identifier: PA2828524232
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1941206
ClinVar RCV Id: RCV002643024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361426.1:p.Ser174Pro
CA360866260
NM_001374497.1:c.520T>C