Canonical Allele Identifier: PA2573170604
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517318
ClinVar RCV Id: RCV002027265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ile1747Phe
CA394314631
NM_000548.5:c.5239A>T