Canonical Allele Identifier: PA1139676852
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 862068
ClinVar RCV Id: RCV001068716 RCV002253767
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys82Arg
CA346729514
NM_000251.3:c.245A>G