Canonical Allele Identifier: PA2827010767
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val1432Ile
CA051988
NM_001318829.2:c.4294G>A