Canonical Allele Identifier: PA915987301
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Pro56Ser
CA375375112
NM_001162427.2:c.166C>T