Canonical Allele Identifier: PA915986892
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 574692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Pro311Ala
CA375368729
NM_001162426.2:c.931C>G