Canonical Allele Identifier: PA2826464775
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246493
ClinVar RCV Id: RCV000235277 RCV002411071 RCV003758739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn547Tyr
CA10584216
NM_001258281.1:c.1639A>T