Canonical Allele Identifier: PA2573164989
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399337
ClinVar RCV Id: RCV001893780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr44Arg
CA346728879
NM_000251.3:c.131C>G