Canonical Allele Identifier: PA241984
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 195531
ClinVar RCV Id: RCV000304805 RCV000398651 RCV000509503 RCV000634201 RCV004537393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Arg863Trp
CA241983
NM_024753.5:c.2587C>T