Canonical Allele Identifier: PA2825957874
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411214
ClinVar Variation Id: 658507
ClinVar RCV Id: RCV000815344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Phe1008Leu
CA036094
NM_001162427.2:c.3024C>G
CA375367134
NM_001162427.2:c.3024C>A
CA375367142
NM_001162427.2:c.3022T>C