Canonical Allele Identifier: PA2825156100
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_000359.1:p.Thr310Ile
CA375368731
NM_000368.5:c.929C>T