Canonical Allele Identifier: PA2827015923
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Tyr1364Cys
CA052633
NM_001318831.2:c.4091A>G