Canonical Allele Identifier: PA1139675280
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 953372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gly1553Asp
CA394305086
NM_000548.5:c.4658G>A