Canonical Allele Identifier: PA2826464822
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro556Leu
CA019478
NM_001258281.1:c.1667C>T
CA3273151128
NM_001258281.1:c.1666_1668delinsTTG
CA3273151130
NM_001258281.1:c.1666_1667delinsTT
CA3273151281
NM_001258281.1:c.1667_1668delinsTT
CA3273151289
NM_001258281.1:c.1667_1668delinsTC
CA3273151298
NM_001258281.1:c.1667_1668delinsTG