Canonical Allele Identifier: PA915986676
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 534416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Met224Leu
CA200900992
NM_001162426.2:c.670A>T
CA375371515
NM_001162426.2:c.670A>C