Canonical Allele Identifier: PA645471861
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr238Asp
CA16611002
NM_000251.3:c.712T>G