Canonical Allele Identifier: PA913193376
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu559Phe
CA346728061
NM_000251.3:c.1677A>C
CA346728062
NM_000251.3:c.1677A>T