Canonical Allele Identifier: PA2741923088
Gene: TBCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2515142
ClinVar RCV Id: RCV003248754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005984.3:p.Gly784Asp
CA401633583
NM_005993.5:c.2351G>A