Canonical Allele Identifier: PA2827009492
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1336Ser
CA050936
NM_001318829.2:c.4006C>A