Canonical Allele Identifier: PA2825916961
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 48800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Glu51Asp
CA005036
NM_001162426.2:c.153A>C
CA375375142
NM_001162426.2:c.153A>T