Canonical Allele Identifier: PA645475402
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229885
ClinVar RCV Id: RCV000215093 RCV003454614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala700Glu
CA10577997
NM_000251.3:c.2099C>A