Canonical Allele Identifier: PA299385
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182589
ClinVar RCV Id: RCV000160626 RCV000198252 RCV000411135 RCV000491808 RCV000656873 RCV000708828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln239Arg
CA022091
NM_000251.3:c.716A>G