Canonical Allele Identifier: PA2825955611
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.His320Gln
CA027069
NM_001162427.2:c.960C>A
CA375367436
NM_001162427.2:c.960C>G