Canonical Allele Identifier: PA357592
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219780
ClinVar RCV Id: RCV000205573 RCV001526104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp597Asn
CA031310
NM_000251.3:c.1789G>A