Canonical Allele Identifier: PA137476
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45973
ClinVar RCV Id: RCV000039208 RCV000260759 RCV000297276 RCV000755231 RCV001273557 RCV004528193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Phe1766Ser
CA137475
NM_022124.6:c.5297T>C