Canonical Allele Identifier: PA2828094755
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49956
ClinVar RCV Id: RCV000043223 RCV002298454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gly1513Ser
CA020963
NM_001363528.2:c.4537G>A