Canonical Allele Identifier: PA2825157500
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2562851
ClinVar RCV Id: RCV003296844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Asp872Tyr
CA375369863
NM_000368.5:c.2614G>T