Canonical Allele Identifier: PA137398
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45931
ClinVar RCV Id: RCV000039165 RCV001103712 RCV000950191 RCV001103711 RCV001272567 RCV001797050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asn1282Ser
CA137396
NM_022124.6:c.3845A>G