Canonical Allele Identifier: PA2828095254
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49484
ClinVar RCV Id: RCV000042744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala1650Pro
CA021872
NM_001363528.2:c.4948G>C