Canonical Allele Identifier: PA2499230060
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171435
ClinVar RCV Id: RCV001524582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys275Arg
CA346732786
NM_000251.3:c.824A>G