Canonical Allele Identifier: PA2573170365
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517946
ClinVar RCV Id: RCV002021394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1508Ser
CA394302795
NM_000548.5:c.4522C>T