Canonical Allele Identifier: PA2827019544
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ile1301Asn
CA10583331
NM_001318832.2:c.3902T>A