Canonical Allele Identifier: PA645480171
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 225684
ClinVar RCV Id: RCV000210956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Gly355Arg
CA10576051
NM_004273.5:c.1063G>A
CA377150553
NM_004273.5:c.1063G>C