Allele Registry

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Canonical Allele Identifier: PA2826465282

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182573

ClinVar RCV Id: RCV000160604 RCV001308489

ClinVar Variation Id: 1787461

ClinVar RCV Id: RCV002425580

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr666Ser	CA020205 NM_001258281.1:c.1997C>G CA346729412 NM_001258281.1:c.1996A>T