Canonical Allele Identifier: PA253886
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 6609
ClinVar RCV Id: RCV000006988 RCV003555950
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004077.1:p.Gly88Glu
CA253885
NM_004086.3:c.263G>A