Canonical Allele Identifier: PA2826464631
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779287
ClinVar RCV Id: RCV002401486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val516Ala
CA346728212
NM_001258281.1:c.1547T>C