Canonical Allele Identifier: PA645506493
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 261780
ClinVar RCV Id: RCV000252032 RCV000861670 RCV001697725 RCV002278217 RCV002518656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Val1139Ala
CA1941516
NM_024753.5:c.3416T>C