Canonical Allele Identifier: PA658801389
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 534457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Leu10Phe
CA375375415
NM_000368.5:c.28C>T