Canonical Allele Identifier: PA915959943
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gln1525Arg
CA394304325
NM_000548.5:c.4574A>G