Canonical Allele Identifier: PA915992212
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162957
ClinVar RCV Id: RCV000150331 RCV001067382 RCV001826807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Arg966His
CA175535
NM_001171934.1:c.2897G>A