Allele Registry

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Canonical Allele Identifier: PA2826463257

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479797

ClinVar RCV Id: RCV000569886 RCV001865717

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly184Arg	CA346732311 NM_001258281.1:c.550G>A CA346732314 NM_001258281.1:c.550G>C