Canonical Allele Identifier: PA2826627323
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821272
ClinVar RCV Id: RCV001015525 RCV002549421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu682Pro
CA346754038
NM_001281492.2:c.2045T>C