Canonical Allele Identifier: PA2825184670
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu1061Met
CA394285548
NM_000548.5:c.3181C>A