Canonical Allele Identifier: PA2579920491
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu701Asp
CA346729237
NM_000251.3:c.2103A>C
CA346729238
NM_000251.3:c.2103A>T