Canonical Allele Identifier: PA2828414555
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405956
ClinVar RCV Id: RCV000458532 RCV000500804 RCV001022474 RCV004000678
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala1435Thr
CA16615031
NM_001370404.1:c.4303G>A