Canonical Allele Identifier: PA2828414134
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ile1313Asn
CA10583331
NM_001370404.1:c.3938T>A