Canonical Allele Identifier: PA2826627290
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 571392
ClinVar RCV Id: RCV000692527 RCV002458235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile675Met
CA346753997
NM_001281492.2:c.2025C>G