Canonical Allele Identifier: PA2826465525
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233932
ClinVar RCV Id: RCV000213912 RCV000690363 RCV003469088
ClinVar Variation Id: 645223
ClinVar RCV Id: RCV000799266 RCV001181432
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr730Ser
CA10578006
NM_001258281.1:c.2188A>T
CA346730139
NM_001258281.1:c.2189C>G