Canonical Allele Identifier: PA211679
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91043
ClinVar RCV Id: RCV000148640 RCV000533753 RCV001016538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val923Glu
CA020923
NM_000251.3:c.2768T>A