Canonical Allele Identifier: PA2579919955
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr668Ile
CA346728965
NM_000251.3:c.2003C>T