Canonical Allele Identifier: PA645506323
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 331839
ClinVar RCV Id: RCV000278829 RCV000336979 RCV004537842 RCV001520464
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Thr161Ala
CA1942424
NM_024753.5:c.481A>G