Canonical Allele Identifier: PA2579919792
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu658Asp
CA346728841
NM_000251.3:c.1974A>C
CA346728843
NM_000251.3:c.1974A>T