Canonical Allele Identifier: PA645471141
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408550
ClinVar RCV Id: RCV002230814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg35Cys
CA16610982
NM_000251.3:c.103C>T