Canonical Allele Identifier: PA2741815516
Gene: THBD HGNC NCBI

Linked Data

ClinVar Variation Id: 2983065
ClinVar RCV Id: RCV003847680 RCV003984437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000352.1:p.Val513Leu
CA408405329
NM_000361.3:c.1537G>T
CA408405331
NM_000361.3:c.1537G>C