Canonical Allele Identifier: PA137267
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45866
ClinVar RCV Id: RCV000039099 RCV000264246 RCV000359188 RCV000755902 RCV001826563 RCV004534821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443068.1:p.Ser436Asn
CA137265
NM_052836.3:c.1307G>A