Canonical Allele Identifier: PA645471861
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408450
ClinVar RCV Id: RCV001026074 RCV002230355 RCV004000771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr238Asp
CA16611002
NM_000251.3:c.712T>G