Canonical Allele Identifier: PA2825577369
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49441
ClinVar RCV Id: RCV000042701 RCV000822377 RCV002336160
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Lys1666Glu
CA021601
NM_001114382.3:c.4996A>G