Canonical Allele Identifier: PA2573167852
Gene: THBD HGNC NCBI

Linked Data

ClinVar Variation Id: 1412347
ClinVar RCV Id: RCV001923205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000352.1:p.Thr504Ser
CA408405376
NM_000361.3:c.1511C>G
CA408405377
NM_000361.3:c.1510A>T