Canonical Allele Identifier: PA103878
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 6609
ClinVar RCV Id: RCV000006988 RCV003555950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128530.1:p.Gly88Glu
CA253885
NM_001135058.2:c.263G>A