Canonical Allele Identifier: PA319239
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro366Leu
CA027020
NM_000368.5:c.1097C>T