Canonical Allele Identifier: PA2829978990
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1113Leu
CA046958
NM_021055.3:c.3338C>T