Canonical Allele Identifier: PA094996
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu93Phe
CA020925
NM_000251.3:c.277C>T