Canonical Allele Identifier: PA658803885
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn263Ser
CA346732512
NM_000251.3:c.788A>G