Canonical Allele Identifier: PA2580304959
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2303740
ClinVar RCV Id: RCV002891412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Gly377Arg
CA377151181
NM_004273.5:c.1129G>C
CA377151185
NM_004273.5:c.1129G>A