Canonical Allele Identifier: PA162584
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 49053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Val178Ile
CA007701
NM_000368.5:c.532G>A