Canonical Allele Identifier: PA915986649
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 64814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Leu116Val
CA007386
NM_001162426.2:c.346T>G