Canonical Allele Identifier: PA915954733
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 640653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile841Met
CA346730761
NM_000251.3:c.2523A>G