Canonical Allele Identifier: PA915987428
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Gly965Asp
CA375367719
NM_001162427.2:c.2894G>A