Canonical Allele Identifier: PA645413443
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Val895Ile
CA034261
NM_000368.5:c.2683G>A