Canonical Allele Identifier: PA253894
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 6613
ClinVar RCV Id: RCV000006992 RCV000710321
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004077.1:p.Ala119Thr
CA253893
NM_004086.3:c.355G>A