Canonical Allele Identifier: PA2826463352
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 632900
ClinVar RCV Id: RCV000780445 RCV001869152 RCV002422667
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala206Thr
CA346732768
NM_001258281.1:c.616G>A