Canonical Allele Identifier: PA2826631298
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485882
ClinVar RCV Id: RCV000561723 RCV001299179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser420Cys
CA346751157
NM_001281493.2:c.1259C>G