Canonical Allele Identifier: PA2826628738
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455276
ClinVar RCV Id: RCV000530800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala1090_Thr1091delinsSerSer
CA658655732
NM_001281492.2:c.3267_3271delinsCTCAT