Canonical Allele Identifier: PA2826634660
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372693
ClinVar RCV Id: RCV001874758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met150Val
CA067532
NM_001281494.2:c.448A>G