Canonical Allele Identifier: PA2826465630
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2820361
ClinVar RCV Id: RCV003760993 RCV004371706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe760Ser
CA346730589
NM_001258281.1:c.2279T>C