Canonical Allele Identifier: PA2826464488
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn481Ser
CA018784
NM_001258281.1:c.1442A>G
CA3273158727
NM_001258281.1:c.1441_1443delinsTCA
CA3273158730
NM_001258281.1:c.1441_1443delinsTCG
CA3273158732
NM_001258281.1:c.1441_1443delinsTCC
CA3273158734
NM_001258281.1:c.1441_1442delinsTC
CA3273158767
NM_001258281.1:c.1442_1443delinsGC