Canonical Allele Identifier: PA2826624682
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729966
ClinVar RCV Id: RCV002454690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe11Ser
CA346734521
NM_001281492.2:c.32T>C