Canonical Allele Identifier: PA2827009208
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile1242Asn
CA10583331
NM_001318829.2:c.3725T>A