Canonical Allele Identifier: PA2828421689
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564709
ClinVar RCV Id: RCV003297141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Lys1701Thr
CA394314672
NM_001370405.1:c.5102A>C