Canonical Allele Identifier: PA2826465035
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly608Arg
CA019825
NM_001258281.1:c.1822G>C