Canonical Allele Identifier: PA2579919679
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2106678
ClinVar RCV Id: RCV003026593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile651Leu
CA346728760
NM_000251.3:c.1951A>C