Canonical Allele Identifier: PA2826463815
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 963222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp313Tyr
CA027070
NM_001258281.1:c.937G>T