Canonical Allele Identifier: PA2499230082
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile666Val
CA346728936
NM_000251.3:c.1996A>G