Canonical Allele Identifier: PA2827003651
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65142
ClinVar RCV Id: RCV000055356
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ser1127Ile
CA019399
NM_001318827.2:c.3380G>T