Canonical Allele Identifier: PA2580234273
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1941206
ClinVar RCV Id: RCV002643024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361428.1:p.Ser68Pro
CA360866260
NM_001374499.1:c.202T>C