Canonical Allele Identifier: PA201937
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 195777
ClinVar RCV Id: RCV000176426 RCV000415806 RCV001135582 RCV000986865 RCV001135581 RCV001085304 RCV001171333 RCV002277374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Leu1002Val
CA201936
NM_024753.5:c.3004C>G