Canonical Allele Identifier: PA2826465928
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met833Ile
CA10582028
NM_001258281.1:c.2499G>T
CA346731621
NM_001258281.1:c.2499G>A
CA346731622
NM_001258281.1:c.2499G>C