Canonical Allele Identifier: PA1139677484
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 843946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met261Ile
CA346732485
NM_000251.3:c.783G>A
CA346732487
NM_000251.3:c.783G>C
CA346732489
NM_000251.3:c.783G>T