Canonical Allele Identifier: PA2579913551
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe286Leu
CA346732848
NM_000251.3:c.856T>C
CA346732853
NM_000251.3:c.858T>A
CA346732854
NM_000251.3:c.858T>G