Canonical Allele Identifier: PA2573170392
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1398100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val1531Met
CA051890
NM_000548.5:c.4591G>A