Canonical Allele Identifier: PA2828420381
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 380381
ClinVar RCV Id: RCV000426687 RCV003626619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro1346Ser
CA16607165
NM_001370405.1:c.4036C>T