Canonical Allele Identifier: PA916023355
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Val350Ile
CA276776626
NM_001318832.2:c.1048G>A