Canonical Allele Identifier: PA2826465598
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489938
ClinVar RCV Id: RCV000580054 RCV001229080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val751Met
CA346730299
NM_001258281.1:c.2251G>A