Canonical Allele Identifier: PA2825182185
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2825177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro669Thr
CA394274455
NM_000548.5:c.2005C>A