Canonical Allele Identifier: PA2579919706
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1783376
ClinVar RCV Id: RCV002421685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn653Lys
CA346728785
NM_000251.3:c.1959T>A
CA346728787
NM_000251.3:c.1959T>G