Canonical Allele Identifier: PA2573165234
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1464359
ClinVar RCV Id: RCV001963445 RCV002425334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn903Tyr
CA037273
NM_000251.3:c.2707A>T