Canonical Allele Identifier: PA2826625122
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525651
ClinVar RCV Id: RCV000629798 RCV002377345 RCV002305519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala167Val
CA346740686
NM_001281492.2:c.500C>T