Canonical Allele Identifier: PA658672453
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 485836
ClinVar RCV Id: RCV000573636 RCV001043758 RCV002497215 RCV004001118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met485Thr
CA346726967
NM_000251.3:c.1454T>C