Canonical Allele Identifier: PA658659647
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Pro585Ser
CA029621
NM_000368.5:c.1753C>T