Canonical Allele Identifier: PA2829976529
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49587
ClinVar RCV Id: RCV000042848 RCV001250499
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu808Ser
CA017395
NM_021055.3:c.2423T>C