Canonical Allele Identifier: PA915987032
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Pro366Leu
CA027020
NM_001162426.2:c.1097C>T