Canonical Allele Identifier: PA103832
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 6613
ClinVar RCV Id: RCV000006992 RCV000710321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128530.1:p.Ala119Thr
CA253893
NM_001135058.2:c.355G>A