Canonical Allele Identifier: PA2827020590
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asn1595Ser
CA021383
NM_001318832.2:c.4784A>G