Canonical Allele Identifier: PA2825086618
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785445
ClinVar RCV Id: RCV002422194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly692_Phe694dup
CA2580067172
NM_000251.3:c.2075_2083dup