Canonical Allele Identifier: PA2828419425
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207676
ClinVar RCV Id: RCV000189915 RCV000490959 RCV000546326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro1066Leu
CA319368
NM_001370405.1:c.3197C>T