Canonical Allele Identifier: PA658667813
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 446444
ClinVar RCV Id: RCV000515672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp1626Ala
CA377139986
NM_022124.6:c.4877A>C