Canonical Allele Identifier: PA231580
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 130651
ClinVar RCV Id: RCV000118723 RCV000244338 RCV000407344 RCV000349862 RCV002277178 RCV001080770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Arg616Cys
CA231579
NM_024753.5:c.1846C>T