Canonical Allele Identifier: PA2580316632
Gene: TBCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2230666
ClinVar RCV Id: RCV002717718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005984.3:p.Gly789Ala
CA401633647
NM_005993.5:c.2366G>C