Canonical Allele Identifier: PA2579920264
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785138
ClinVar RCV Id: RCV002421887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val686Ile
CA346729154
NM_000251.3:c.2056G>A