Canonical Allele Identifier: PA916010256
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 828155
ClinVar RCV Id: RCV001028033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Ile168Ser
CA377144212
NM_004273.5:c.503T>G