Canonical Allele Identifier: PA299347
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe42Leu
CA017708
NM_000251.3:c.126C>G
CA027356
NM_000251.3:c.126C>A
CA346728855
NM_000251.3:c.124T>C