Allele Registry

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Canonical Allele Identifier: PA2826465242

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2064560

ClinVar RCV Id: RCV002953513

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly655Arg	CA346729346 NM_001258281.1:c.1963G>A CA346729347 NM_001258281.1:c.1963G>C