Allele Registry

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Canonical Allele Identifier: PA645472103

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408483

ClinVar RCV Id: RCV000473312 RCV000587461 RCV001026892

ClinVar Variation Id: 921168

ClinVar RCV Id: RCV001180427 RCV001316892

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu262Asp	CA040426 NM_000251.3:c.786G>C CA16611010 NM_000251.3:c.786G>T