Canonical Allele Identifier: PA658672358
Gene: MSH2 HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr441Ser
CA346724617
NM_000251.3:c.1321A>T
CA346724620
NM_000251.3:c.1322C>G