Canonical Allele Identifier: PA915984139
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn61Thr
CA346730352
NM_001258281.1:c.182A>C
CA3273132497
NM_001258281.1:c.182_183delinsCA
CA3273132499
NM_001258281.1:c.182_183delinsCG
CA3273132500
NM_001258281.1:c.182_183delinsCC