Canonical Allele Identifier: PA332433
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile906Thr
CA020898
NM_000251.3:c.2717T>C