Canonical Allele Identifier: PA2826463316
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn197Ser
CA346732512
NM_001258281.1:c.590A>G