Canonical Allele Identifier: PA915986890
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 655773
ClinVar RCV Id: RCV000812022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Thr310Ile
CA375368731
NM_001162426.2:c.929C>T