Canonical Allele Identifier: PA2830168516
Gene: CHST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1012668
ClinVar RCV Id: RCV001310744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569735.1:p.Cys374del