Canonical Allele Identifier: PA2827004085
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207752
ClinVar RCV Id: RCV000190029 RCV000644243 RCV001021792 RCV003996895
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Gly1253Asp
CA050325
NM_001318827.2:c.3758G>A