Canonical Allele Identifier: PA2580304963
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920312
ClinVar RCV Id: RCV002630517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Gly390Asp
CA377151506
NM_004273.5:c.1169G>A