Canonical Allele Identifier: PA2828091285
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser526Asn
CA031083
NM_001363528.2:c.1577G>A