Canonical Allele Identifier: PA2829972681
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro378Leu
CA013884
NM_021055.3:c.1133C>T