Canonical Allele Identifier: PA092631
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 459288
ClinVar RCV Id: RCV000550901 RCV001128710 RCV001128711 RCV001258267 RCV001572659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Pro753Leu
CA1941879
NM_024753.5:c.2258C>T