Allele Registry

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Canonical Allele Identifier: PA2826466056

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455585

ClinVar RCV Id: RCV000558906 RCV001755788 RCV001181312

ClinVar Variation Id: 921415

ClinVar RCV Id: RCV001180785

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr867Ser	CA346732271 NM_001258281.1:c.2599A>T CA346732277 NM_001258281.1:c.2600C>G