Canonical Allele Identifier: PA915986922
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823399
ClinVar RCV Id: RCV001019621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Pro323Leu
CA375368653
NM_001162426.2:c.968C>T