Canonical Allele Identifier: PA128735
Gene: THBD HGNC NCBI

Linked Data

ClinVar Variation Id: 29903
ClinVar RCV Id: RCV000022787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000352.1:p.Arg403Ser
CA128733
NM_000361.3:c.1209G>T
CA408406029
NM_000361.3:c.1209G>C