Canonical Allele Identifier: PA2826463656
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127625
ClinVar RCV Id: RCV000115492 RCV000467692 RCV000562717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn277Asp
CA016891
NM_001258281.1:c.829A>G