Canonical Allele Identifier: PA2828092508
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237997
ClinVar RCV Id: RCV000234558 RCV002450675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asn859Thr
CA10583312
NM_001363528.2:c.2576A>C