Canonical Allele Identifier: PA2825573244
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro436Leu
CA319435
NM_001114382.3:c.1307C>T