Canonical Allele Identifier: PA2826465075
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly617Val
CA339026
NM_001258281.1:c.1850G>T