Canonical Allele Identifier: PA645506434
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 261770
ClinVar RCV Id: RCV000253498 RCV000516123 RCV001589274 RCV001854967
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Arg672Trp
CA1941956
NM_024753.5:c.2014C>T