Canonical Allele Identifier: PA2827020237
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232172
ClinVar RCV Id: RCV004520855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gly1495Ala
CA394305032
NM_001318832.2:c.4484G>C