Canonical Allele Identifier: PA2825788400
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 226529
ClinVar RCV Id: RCV000215337 RCV000387678 RCV000755937 RCV000787992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128530.1:p.Asp281Asn
CA7143202
NM_001135058.2:c.841G>A