Canonical Allele Identifier: PA913193046
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 633311
ClinVar RCV Id: RCV000781554 RCV001370341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu223Val
CA346731750
NM_000251.3:c.667C>G