Canonical Allele Identifier: PA2826465616
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 821316
ClinVar RCV Id: RCV001015613 RCV001860800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val755Ile
CA346730515
NM_001258281.1:c.2263G>A