Canonical Allele Identifier: PA1139735772
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 885986
ClinVar RCV Id: RCV001117910 RCV002558162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Ala219Val
CA8175437
NM_021615.5:c.656C>T