Canonical Allele Identifier: PA2826465694
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys777Ser
CA346730774
NM_001258281.1:c.2329T>A
CA346730781
NM_001258281.1:c.2330G>C