Canonical Allele Identifier: PA137377
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45919
ClinVar RCV Id: RCV000039152 RCV000891539 RCV001105553 RCV001105554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Met1160Ile
CA137376
NM_022124.6:c.3480G>T
CA377152310
NM_022124.6:c.3480G>A
CA377152313
NM_022124.6:c.3480G>C