Canonical Allele Identifier: PA2829983278
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2771708
ClinVar RCV Id: RCV003512766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Met1672Ile
CA394312590
NM_021055.3:c.5016G>T
CA394312593
NM_021055.3:c.5016G>C
CA394312596
NM_021055.3:c.5016G>A