Canonical Allele Identifier: PA891846898
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn127Thr
CA346730352
NM_000251.3:c.380A>C
CA3273132497
NM_000251.3:c.380_381delinsCA
CA3273132499
NM_000251.3:c.380_381delinsCG
CA3273132500
NM_000251.3:c.380_381delinsCC