Canonical Allele Identifier: PA2826465294
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile669Val
CA020218
NM_001258281.1:c.2005A>G