Canonical Allele Identifier: PA2826463168
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 567200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala164Gly
CA346731904
NM_001258281.1:c.491C>G