Canonical Allele Identifier: PA155816
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.His732Tyr
CA006123
NM_000368.5:c.2194C>T