Canonical Allele Identifier: PA2829515143
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 813819
ClinVar RCV Id: RCV001004791 RCV003558639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004077.1:p.Ile372Thr
CA389348313
NM_004086.3:c.1115T>C