Canonical Allele Identifier: PA645506484
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 331824
ClinVar RCV Id: RCV000281585 RCV000387559 RCV000756834 RCV004537838 RCV001859969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Arg939Trp
CA1941692
NM_024753.5:c.2815C>T