Canonical Allele Identifier: PA645434814
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Asp1512Asn
CA16614792
NM_000548.5:c.4534G>A