Canonical Allele Identifier: PA645432300
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro672Leu
CA16615063
NM_000548.5:c.2015C>T