Canonical Allele Identifier: PA2825576974
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_001107854.1:p.Gly1556Ser
CA020963
NM_001114382.3:c.4666G>A