Canonical Allele Identifier: PA2828061145
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Arg906Trp
CA035767
NM_001362177.1:c.2716C>T