Canonical Allele Identifier: PA2826464470
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 485840
ClinVar RCV Id: RCV000570016 RCV003459387 RCV003767224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val476Ala
CA346727945
NM_001258281.1:c.1427T>C