Canonical Allele Identifier: PA2825917943
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Asn531Tyr
CA029180
NM_001162426.2:c.1591A>T