Canonical Allele Identifier: PA137371
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45916
ClinVar RCV Id: RCV000039149 RCV000724083 RCV001075026 RCV001272560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ile1121Phe
CA137370
NM_022124.6:c.3361A>T