Canonical Allele Identifier: PA2827020973
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517318
ClinVar RCV Id: RCV002027265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ile1691Phe
CA394314631
NM_001318832.2:c.5071A>T