Canonical Allele Identifier: PA916029211
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_001334649.1:p.Ile437Thr
CA389348313
NM_001347720.2:c.1310T>C