Canonical Allele Identifier: PA2828410727
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val319Met
CA394315689
NM_001370404.1:c.955G>A