Canonical Allele Identifier: PA2579917594
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr526Ser
CA346727834
NM_000251.3:c.1576A>T
CA346727836
NM_000251.3:c.1577C>G