Canonical Allele Identifier: PA645413178
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro366Ala
CA16612486
NM_000368.5:c.1096C>G