Canonical Allele Identifier: PA2828060389
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 646276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Arg585Ser
CA375361019
NM_001362177.1:c.1753C>A