Canonical Allele Identifier: PA2826465713
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220024
ClinVar RCV Id: RCV000204877 RCV000491044 RCV001570632 RCV003997603
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala782Ser
CA036472
NM_001258281.1:c.2344G>T