Canonical Allele Identifier: PA2826465117
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly626Glu
CA10588345
NM_001258281.1:c.1877G>A