Canonical Allele Identifier: PA2826462847
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1797805
ClinVar RCV Id: RCV002440055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr32Asp
CA346729611
NM_001258281.1:c.94T>G