Canonical Allele Identifier: PA645506471
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 261776
ClinVar RCV Id: RCV000252244 RCV000861928 RCV001134203 RCV001134204 RCV001705374
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Arg867His
CA1941767
NM_024753.5:c.2600G>A