Canonical Allele Identifier: PA2828418872
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467957
ClinVar RCV Id: RCV000559686 RCV002438411 RCV003237913 RCV003999273
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala894Val
CA040893
NM_001370405.1:c.2681C>T