Canonical Allele Identifier: PA645506483
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 331825
ClinVar RCV Id: RCV000334319 RCV000372660 RCV001861133 RCV002480176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Arg926Gln
CA1941701
NM_024753.5:c.2777G>A