Canonical Allele Identifier: PA092662
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 198257
ClinVar RCV Id: RCV000179530 RCV000724482 RCV001087340 RCV001132638 RCV000986867 RCV001132639 RCV004537489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Thr231Ser
CA246806
NM_024753.5:c.691A>T