Canonical Allele Identifier: PA264751
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1379Leu
CA019991
NM_000548.5:c.4136C>T