Canonical Allele Identifier: PA1139680062
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 960712
ClinVar RCV Id: RCV001234287 RCV002411866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly614Glu
CA346728398
NM_000251.3:c.1841G>A