Canonical Allele Identifier: PA092624
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 30935
ClinVar RCV Id: RCV000023924 RCV000681870 RCV000685092 RCV000763456 RCV000857219 RCV000786982 RCV001003236 RCV001074967 RCV001328175 RCV002251925 RCV004528134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Pro209Leu
CA259949
NM_024753.5:c.626C>T