Canonical Allele Identifier: PA2828061201
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Leu924Phe
CA319263
NM_001362177.1:c.2770C>T