Canonical Allele Identifier: PA2826465913
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455581
ClinVar RCV Id: RCV000539916 RCV000561718 RCV001357777 RCV003459180 RCV003441913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro829Leu
CA346731558
NM_001258281.1:c.2486C>T