Canonical Allele Identifier: PA2573167868
Gene: THBD HGNC NCBI

Linked Data

ClinVar Variation Id: 1370926
ClinVar RCV Id: RCV001878742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000352.1:p.Val566Gly
CA9787510
NM_000361.3:c.1697T>G