Canonical Allele Identifier: PA2828061040
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 365510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Ala868Ser
CA035133
NM_001362177.1:c.2602G>T