Canonical Allele Identifier: PA1139719800
Gene: TBCD HGNC NCBI

Linked Data

ClinVar Variation Id: 973248
ClinVar RCV Id: RCV001249656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005984.3:p.Glu769del
CA2279278080
NM_005993.5:c.2305_2307del