Canonical Allele Identifier: PA335912
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216349
ClinVar RCV Id: RCV000195748 RCV000579733 RCV002307442 RCV003997018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile691Thr
CA033486
NM_000251.3:c.2072T>C