Canonical Allele Identifier: PA645476302
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met899Ile
CA10582028
NM_000251.3:c.2697G>T
CA346731621
NM_000251.3:c.2697G>A
CA346731622
NM_000251.3:c.2697G>C