Canonical Allele Identifier: PA2826465915
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187208
ClinVar RCV Id: RCV000166913 RCV000484021 RCV001058479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro829Arg
CA020884
NM_001258281.1:c.2486C>G