Canonical Allele Identifier: PA2829973055
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro436Leu
CA319435
NM_021055.3:c.1307C>T