Canonical Allele Identifier: PA137359
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45910
ClinVar RCV Id: RCV000039143 RCV001243389 RCV001826568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val1045Leu
CA137358
NM_022124.6:c.3133G>T
CA377143098
NM_022124.6:c.3133G>C