Canonical Allele Identifier: PA2826464707
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1404541
ClinVar RCV Id: RCV001927763 RCV003585152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu533Val
CA46700085
NM_001258281.1:c.1597T>G