Canonical Allele Identifier: PA2825438514
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207684
ClinVar RCV Id: RCV000934634 RCV001022397 RCV001427433
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Thr1395Ser
CA051006
NM_001077183.3:c.4184C>G
CA394301849
NM_001077183.3:c.4183A>T