Canonical Allele Identifier: PA2826463484
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91243
ClinVar RCV Id: RCV000076748 RCV000115547 RCV000148633 RCV000656876 RCV001084038 RCV001193245 RCV004542749 RCV003492427
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala239Thr
CA022539
NM_001258281.1:c.715G>A