Canonical Allele Identifier: PA645510705
Gene: THBD HGNC NCBI

Linked Data

ClinVar Variation Id: 438664
ClinVar RCV Id: RCV000505639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000352.1:p.Thr571Met
CA408404966
NM_000361.3:c.1712C>T