Canonical Allele Identifier: PA2579920973
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met729Leu
CA346729390
NM_000251.3:c.2185A>C
CA346729392
NM_000251.3:c.2185A>T