Canonical Allele Identifier: PA2579913334
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val273Leu
CA346732773
NM_000251.3:c.817G>C
CA346732774
NM_000251.3:c.817G>T