Canonical Allele Identifier: PA2826628258
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1994636
ClinVar RCV Id: RCV002791280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg946_Pro947insSer
CA2580066980
NM_001281492.2:c.2838_2839insAGC