Canonical Allele Identifier: PA2579920765
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser717Arg
CA346729319
NM_000251.3:c.2149A>C
CA346729323
NM_000251.3:c.2151T>A
CA346729324
NM_000251.3:c.2151T>G