Canonical Allele Identifier: PA645433076
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238014
ClinVar Variation Id: 823131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Asn1064Lys
CA044699
NM_000548.5:c.3192C>A
CA394285620
NM_000548.5:c.3192C>G