Allele Registry

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Canonical Allele Identifier: PA2826465648

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 579266

ClinVar RCV Id: RCV000702508 RCV003999729

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu766Asp	CA036265 NM_001258281.1:c.2298G>T CA346730659 NM_001258281.1:c.2298G>C