Canonical Allele Identifier: PA2826464369
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe453Leu
CA346727792
NM_001258281.1:c.1357T>C
CA346727797
NM_001258281.1:c.1359T>A
CA346727798
NM_001258281.1:c.1359T>G