Canonical Allele Identifier: PA2741815537
Gene: THBD HGNC NCBI

Linked Data

ClinVar Variation Id: 2857711
ClinVar RCV Id: RCV003703993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000352.1:p.His565Arg
CA408404999
NM_000361.3:c.1694A>G