Canonical Allele Identifier: PA2826465003
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr602Ile
CA346728965
NM_001258281.1:c.1805C>T