Canonical Allele Identifier: PA2826465840
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246206
ClinVar RCV Id: RCV000235500 RCV002229806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr808Asp
CA10584225
NM_001258281.1:c.2422T>G