Canonical Allele Identifier: PA913198702
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 596968
ClinVar RCV Id: RCV000732952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Gln396Arg
CA209479393
NM_004273.5:c.1187A>G