Canonical Allele Identifier: PA2826464986
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met597Ile
CA338389
NM_001258281.1:c.1791G>A
CA346728905
NM_001258281.1:c.1791G>C
CA346728907
NM_001258281.1:c.1791G>T