Canonical Allele Identifier: PA645433674
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 389507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1263Leu
CA16607157
NM_000548.5:c.3788C>T