Canonical Allele Identifier: PA645472049
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met261Val
CA16611007
NM_000251.3:c.781A>G