Canonical Allele Identifier: PA2579920372
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys693Ser
CA346729191
NM_000251.3:c.2077T>A
CA346729194
NM_000251.3:c.2078G>C