Canonical Allele Identifier: PA2825956819
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Trp675Arg
CA030669
NM_001162426.2:c.2023T>A
CA375361293
NM_001162426.2:c.2023T>C