Canonical Allele Identifier: PA2826465696
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 942502
ClinVar RCV Id: RCV001212501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys777Arg
CA346730776
NM_001258281.1:c.2329T>C