Canonical Allele Identifier: PA2827009652
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1382Ser
CA020513
NM_001318829.2:c.4144C>T