Canonical Allele Identifier: PA1139676307
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 947130
ClinVar RCV Id: RCV001218133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe42Tyr
CA346728858
NM_000251.3:c.125T>A