Canonical Allele Identifier: PA2828414982
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49464
ClinVar RCV Id: RCV000042724 RCV001508405 RCV001852888 RCV003162357
ClinVar Variation Id: 2728549
ClinVar RCV Id: RCV003513445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly1551Arg
CA021000
NM_001370404.1:c.4651G>A
CA394307955
NM_001370404.1:c.4651G>C