Canonical Allele Identifier: PA2827005151
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Phe1554Tyr
CA10583340
NM_001318827.2:c.4661T>A