Canonical Allele Identifier: PA2825919337
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Arg1026Trp
CA035767
NM_001162426.2:c.3076C>T