Canonical Allele Identifier: PA2741815007
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564709
ClinVar RCV Id: RCV003297141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Lys1748Thr
CA394314672
NM_000548.5:c.5243A>C