Canonical Allele Identifier: PA299339
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182570
ClinVar RCV Id: RCV000160601 RCV000590168 RCV000796598 RCV002247555 RCV003998477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile704Val
CA020041
NM_000251.3:c.2110A>G