Canonical Allele Identifier: PA357678
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220448
ClinVar RCV Id: RCV000206288 RCV000235898 RCV000214778 RCV000781988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg55Gln
CA029952
NM_000251.3:c.164G>A