Canonical Allele Identifier: PA264639
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65215
ClinVar RCV Id: RCV000055434 RCV000989440
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1653Pro
CA021390
NM_000548.5:c.4957T>C