Canonical Allele Identifier: PA2825577222
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asn1628Ser
CA021383
NM_001114382.3:c.4883A>G