Canonical Allele Identifier: PA1139682289
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 842450
ClinVar RCV Id: RCV001044876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu888Val
CA346731447
NM_000251.3:c.2662C>G