Canonical Allele Identifier: PA645506425
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 261768
ClinVar RCV Id: RCV000249020 RCV000861850 RCV001135808 RCV001135809 RCV001418739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Val559Gly
CA1942041
NM_024753.5:c.1676T>G