Canonical Allele Identifier: PA658672004
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479846
ClinVar RCV Id: RCV000571615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln298Arg
CA346732927
NM_000251.3:c.893A>G