Canonical Allele Identifier: PA2579911107
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met141Leu
CA346730438
NM_000251.3:c.421A>C
CA346730439
NM_000251.3:c.421A>T
CA3273116224
NM_000251.3:c.421_423delinsTTA
CA3273116353
NM_000251.3:c.421_423delinsCTT
CA3273116388
NM_000251.3:c.421_423delinsCTC
CA3273116405
NM_000251.3:c.421_423delinsCTA