Canonical Allele Identifier: PA2826464704
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val532Met
CA031369
NM_001258281.1:c.1594G>A