Canonical Allele Identifier: PA645506500
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 331819
ClinVar RCV Id: RCV000297705 RCV003151031 RCV001812869 RCV000407838 RCV000861564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Asp1305Gly
CA1941338
NM_024753.5:c.3914A>G