Canonical Allele Identifier: PA658678574
Gene: TTC21B HGNC NCBI
ClinVar RCV:
RCV000516140
ClinVar Variation:
446646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079029.3:p.Pro466His
CA349062475
NM_024753.5:c.1397C>A