Canonical Allele Identifier: PA2827404382
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_001334649.1:p.Gly153Glu
CA253885
NM_001347720.2:c.458G>A