Canonical Allele Identifier: PA2828415424
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000279
ClinVar RCV Id: RCV001751562 RCV001296392 RCV003294205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Met1671Thr
CA054058
NM_001370404.1:c.5012T>C