Canonical Allele Identifier: PA137555
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46021
ClinVar RCV Id: RCV000039257 RCV000260501 RCV000353028 RCV000764921 RCV001244627 RCV001275584 RCV004528196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg2304Gln
CA137554
NM_022124.6:c.6911G>A