Canonical Allele Identifier: PA2579920380
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe694Leu
CA46702559
NM_000251.3:c.2080T>C
CA346729203
NM_000251.3:c.2082T>A
CA346729204
NM_000251.3:c.2082T>G