Canonical Allele Identifier: PA2825956979
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692395
ClinVar RCV Id: RCV002258532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Phe706Ser
CA375361009
NM_001162426.2:c.2117T>C