Canonical Allele Identifier: PA331568
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91056
ClinVar RCV Id: RCV000693356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr98Cys
CA020980
NM_000251.3:c.293A>G