Canonical Allele Identifier: PA2827010446
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517318
ClinVar RCV Id: RCV002027265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile1632Phe
CA394314631
NM_001318829.2:c.4894A>T