Canonical Allele Identifier: PA658659373
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Thr44Ala
CA375375194
NM_000368.5:c.130A>G