Canonical Allele Identifier: PA2826465878
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418714
ClinVar RCV Id: RCV000485019 RCV000549838 RCV001016216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile818Thr
CA16617611
NM_001258281.1:c.2453T>C