Canonical Allele Identifier: PA2499245066
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008271
ClinVar RCV Id: RCV001305575 RCV002411978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro59Arg
CA346735007
NM_001281492.2:c.176C>G