Canonical Allele Identifier: PA2827010708
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207684
ClinVar RCV Id: RCV000934634 RCV001022397 RCV001427433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr1347Ser
CA051006
NM_001318829.2:c.4040C>G
CA394301849
NM_001318829.2:c.4039A>T