Canonical Allele Identifier: PA2826464992
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 820464
ClinVar RCV Id: RCV001013958 RCV003318653 RCV001347871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His599Tyr
CA346728925
NM_001258281.1:c.1795C>T