Canonical Allele Identifier: PA645414159
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Leu994Phe
CA319263
NM_001162427.2:c.2980C>T