Canonical Allele Identifier: PA2826463371
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1357042
ClinVar RCV Id: RCV001880585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu211Ser
CA346732800
NM_001258281.1:c.632T>C