Canonical Allele Identifier: PA2573280978
Gene: CHST6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1382293
ClinVar RCV Id: RCV001922179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067628.1:p.Phe178Val
CA396792412
NM_021615.5:c.532T>G