Canonical Allele Identifier: PA2826464876
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422780
ClinVar RCV Id: RCV000482793 RCV000816301 RCV001013660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser571Cys
CA16617596
NM_001258281.1:c.1712C>G