Canonical Allele Identifier: PA915965099
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 655766
ClinVar RCV Id: RCV000812013 RCV001257480 RCV002453838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val809Ala
CA069038
NM_000179.3:c.2426T>C