Canonical Allele Identifier: PA2828421426
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207758
ClinVar RCV Id: RCV000190039 RCV001084596 RCV002336507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Cys1637Tyr
CA053573
NM_001370405.1:c.4910G>A