Canonical Allele Identifier: PA169211
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly71Arg
CA020066
NM_000251.3:c.211G>C
CA346729065
NM_000251.3:c.211G>A
CA2580067374
NM_000251.3:c.210_211delinsCC