Canonical Allele Identifier: PA2827020435
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468115
ClinVar RCV Id: RCV002330908 RCV000547996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Tyr1552Cys
CA052633
NM_001318832.2:c.4655A>G