Canonical Allele Identifier: PA2828092607
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49586
ClinVar RCV Id: RCV000042847 RCV000201152 RCV002433527
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala889Val
CA017841
NM_001363528.2:c.2666C>T