Canonical Allele Identifier: PA299357
Gene: MSH2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met779Ile
CA020479
NM_000251.3:c.2337G>A
CA346729931
NM_000251.3:c.2337G>C
CA346729932
NM_000251.3:c.2337G>T