Canonical Allele Identifier: PA287456
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met141Val
CA021148
NM_000251.3:c.421A>G
CA3273116079
NM_000251.3:c.421_423delinsGTT
CA3273116283
NM_000251.3:c.421_423delinsGTC
CA3273116457
NM_000251.3:c.421_423delinsGTA