Canonical Allele Identifier: PA2828094570
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1463Trp
CA276754888
NM_001363528.2:c.4387C>T