Canonical Allele Identifier: PA658805065
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1215Leu
CA276749978
NM_000548.5:c.3644C>T