Canonical Allele Identifier: PA658659661
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Thr624Ile
CA029981
NM_000368.5:c.1871C>T