Canonical Allele Identifier: PA2828415451
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406062
ClinVar RCV Id: RCV000658430 RCV001086881 RCV002257695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Met1677Val
CA054307
NM_001370404.1:c.5029A>G