Canonical Allele Identifier: PA658678606
Gene: TTC21B HGNC NCBI

Linked Data

ClinVar Variation Id: 459287
ClinVar RCV Id: RCV000534023 RCV002483379 RCV002527695 RCV001336665 RCV004541651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Asn752Ser
CA1941882
NM_024753.5:c.2255A>G