Canonical Allele Identifier: PA2826628118
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455226
ClinVar RCV Id: RCV000547617 RCV000562916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser868Cys
CA346756385
NM_001281492.2:c.2603C>G