Canonical Allele Identifier: PA2827020483
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536102
ClinVar RCV Id: RCV000644406 RCV001023169 RCV004004050
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala1566Thr
CA052965
NM_001318832.2:c.4696G>A