Canonical Allele Identifier: PA2580186399
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730489
ClinVar RCV Id: RCV002320957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Cys987Gly
CA346758754
NM_001281492.2:c.2959T>G