Canonical Allele Identifier: PA191007
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90555
ClinVar RCV Id: RCV000164456 RCV000524331 RCV000662913 RCV000780454 RCV001564699
ClinVar Variation Id: 1503335
ClinVar RCV Id: RCV002022770 RCV003316859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp38Glu
CA017363
NM_000251.3:c.114C>G
CA346728812
NM_000251.3:c.114C>A