Canonical Allele Identifier: PA2828095151
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535944
ClinVar RCV Id: RCV000644178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asp1624Asn
CA394311729
NM_001363528.2:c.4870G>A