Canonical Allele Identifier: PA658659835
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 486574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Met1004Thr
CA035603
NM_000368.5:c.3011T>C