Canonical Allele Identifier: PA2826633782
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2105087
ClinVar RCV Id: RCV003041851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile981Phe
CA346761302
NM_001281493.2:c.2941A>T