Canonical Allele Identifier: PA092571
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 194432
ClinVar RCV Id: RCV000174799 RCV000755750 RCV001078741 RCV000764280 RCV001134339
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.His566Arg
CA240377
NM_024753.5:c.1697A>G