Canonical Allele Identifier: PA2828420726
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala1446Thr
CA020493
NM_001370405.1:c.4336G>A