Canonical Allele Identifier: PA2579923546
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000242.1:p.Glu881Asp
NM_000251.3:c.2643A>C

NM_000251.3:c.2643A>T