Canonical Allele Identifier: PA2829973621
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ser526Asn
CA031083
NM_021055.3:c.1577G>A