Canonical Allele Identifier: PA658678561
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 446647
ClinVar RCV Id: RCV000516004 RCV001304507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Ala235Pro
CA1942372
NM_024753.5:c.703G>C