Canonical Allele Identifier: PA645472626
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser297Arg
CA10584210
NM_000251.3:c.891C>G
CA346732917
NM_000251.3:c.889A>C
CA346732923
NM_000251.3:c.891C>A