Canonical Allele Identifier: PA2827020224
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Val1491Ile
CA051988
NM_001318832.2:c.4471G>A