Canonical Allele Identifier: PA2826464659
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 419601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val523Ile
CA16617588
NM_001258281.1:c.1567G>A