Canonical Allele Identifier: PA2580428569
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2325899
ClinVar RCV Id: RCV002906868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Leu184Val
CA8175467
NM_021615.5:c.550C>G