Canonical Allele Identifier: PA645472137
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn263Lys
CA10582001
NM_000251.3:c.789T>G
CA346732518
NM_000251.3:c.789T>A