Canonical Allele Identifier: PA2826464202
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 571519
ClinVar RCV Id: RCV000692689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro406Ala
CA346726782
NM_001258281.1:c.1216C>G