Canonical Allele Identifier: PA645413069
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411244
ClinVar RCV Id: RCV000474214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Lys121Met
CA16612651
NM_000368.5:c.362A>T