Canonical Allele Identifier: PA645506450
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 331829
ClinVar RCV Id: RCV000263172 RCV000634198 RCV000756833 RCV000318231 RCV004537839 RCV002521311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Val743Ile
CA1941888
NM_024753.5:c.2227G>A