Canonical Allele Identifier: PA2826462853
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483726
ClinVar RCV Id: RCV000564120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg33Lys
CA346729619
NM_001258281.1:c.98G>A