Canonical Allele Identifier: PA2828092560
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486642
ClinVar RCV Id: RCV000571394 RCV001047205 RCV004001160
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro874Leu
CA276741554
NM_001363528.2:c.2621C>T