Canonical Allele Identifier: PA2826465055
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483690
ClinVar RCV Id: RCV000568876 RCV001858298 RCV003451248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg614Pro
CA346729131
NM_001258281.1:c.1841G>C