Canonical Allele Identifier: PA2826463315
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn197Lys
CA10582001
NM_001258281.1:c.591T>G
CA346732518
NM_001258281.1:c.591T>A