Canonical Allele Identifier: PA658659879
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Arg1062Gln
CA036127
NM_000368.5:c.3185G>A