Canonical Allele Identifier: PA2828412780
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2100443
ClinVar RCV Id: RCV003025893
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Phe908Leu
CA394279532
NM_001370404.1:c.2722T>C
CA394279543
NM_001370404.1:c.2724T>G
CA394279545
NM_001370404.1:c.2724T>A