Canonical Allele Identifier: PA645472159
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428563
ClinVar RCV Id: RCV000492013 RCV000629850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala266Thr
CA346732742
NM_000251.3:c.796G>A