Canonical Allele Identifier: PA2826465124
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 393457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys627Tyr
CA16609274
NM_001258281.1:c.1880G>A