Canonical Allele Identifier: PA264702
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65305

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Asp1535Val
CA020759
NM_000548.5:c.4604A>T