Canonical Allele Identifier: PA231582
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 130656
ClinVar RCV Id: RCV000118728 RCV001131126 RCV001131125 RCV004529986 RCV001078717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Pro1266Leu
CA231581
NM_024753.5:c.3797C>T