Canonical Allele Identifier: PA658659695
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Thr677Ile
CA030690
NM_000368.5:c.2030C>T