Canonical Allele Identifier: PA2826465701
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2755828
ClinVar RCV Id: RCV003593801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys779Gln
CA346730796
NM_001258281.1:c.2335A>C