Canonical Allele Identifier: PA2828415426
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2771708
ClinVar RCV Id: RCV003512766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Met1671Ile
CA394312590
NM_001370404.1:c.5013G>T
CA394312593
NM_001370404.1:c.5013G>C
CA394312596
NM_001370404.1:c.5013G>A