Canonical Allele Identifier: PA2828409801
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207655
ClinVar RCV Id: RCV000189881 RCV000467572 RCV002314773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Thr36Ala
CA028094
NM_001370404.1:c.106A>G