Canonical Allele Identifier: PA2826463304
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met195Val
CA16611007
NM_001258281.1:c.583A>G