Canonical Allele Identifier: PA915966652
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 640478
ClinVar RCV Id: RCV000793508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr238Phe
CA346732076
NM_000251.3:c.713A>T