Canonical Allele Identifier: PA2826632466
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453169
ClinVar RCV Id: RCV003182624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu694Ser
CA346756372
NM_001281493.2:c.2081T>C