Allele Registry

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Canonical Allele Identifier: PA169211

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142708

ClinVar RCV Id: RCV000132075 RCV000535324 RCV000503476 RCV000985801 RCV001353465 RCV003453090

ClinVar Variation Id: 2108540

ClinVar RCV Id: RCV003017672

ClinVar Variation Id: 3065347

ClinVar RCV Id: RCV003990424

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly71Arg	CA020066 NM_000251.3:c.211G>C CA346729065 NM_000251.3:c.211G>A CA2580067374 NM_000251.3:c.210_211delinsCC