Canonical Allele Identifier: PA658680480
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val319Met
CA394315689
NM_000548.5:c.955G>A