Canonical Allele Identifier: PA2579911622
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg171Ser
CA346730721
NM_000251.3:c.513G>C
CA346730723
NM_000251.3:c.513G>T