Canonical Allele Identifier: PA645475467
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408499
ClinVar RCV Id: RCV000469918 RCV000481613 RCV000491178 RCV004000781 RCV004533186
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile708Val
CA034231
NM_000251.3:c.2122A>G