Canonical Allele Identifier: PA2826631660
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_001268422.1:p.Val507Ala
CA069038
NM_001281493.2:c.1520T>C