Canonical Allele Identifier: PA658739902
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 495769
ClinVar RCV Id: RCV000589997 RCV000772497 RCV002530899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln910Arg
CA346731831
NM_000251.3:c.2729A>G