Canonical Allele Identifier: PA338219
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 216768
ClinVar RCV Id: RCV000198827 RCV000417538 RCV001134079 RCV001134078 RCV002492924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Val1075Leu
CA338218
NM_024753.5:c.3223G>C