Canonical Allele Identifier: PA915984383
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90513
ClinVar RCV Id: RCV000076008 RCV000490568 RCV002399451
ClinVar Variation Id: 561171
ClinVar RCV Id: RCV000680197
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro283Arg
CA016981
NM_001258281.1:c.848C>G
CA658822113
NM_001258281.1:c.848_849delinsGC