Canonical Allele Identifier: PA2826465867
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1377625
ClinVar RCV Id: RCV001889948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly814Ala
CA346731331
NM_001258281.1:c.2441G>C