Canonical Allele Identifier: PA2827020834
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2771708
ClinVar RCV Id: RCV003512766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Met1659Ile
CA394312590
NM_001318832.2:c.4977G>T
CA394312593
NM_001318832.2:c.4977G>C
CA394312596
NM_001318832.2:c.4977G>A