Canonical Allele Identifier: PA2826464946
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1783441
ClinVar RCV Id: RCV002421750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp588Gly
CA346728797
NM_001258281.1:c.1763A>G