Canonical Allele Identifier: PA2825956192
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Asn481Tyr
CA029180
NM_001162427.2:c.1441A>T