Canonical Allele Identifier: PA2573165254
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413129
ClinVar RCV Id: RCV001943368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile926Leu
CA346732147
NM_000251.3:c.2776A>C