Canonical Allele Identifier: PA658672002
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479808
ClinVar RCV Id: RCV000562750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe294Cys
CA346732899
NM_000251.3:c.881T>G