Canonical Allele Identifier: PA916029219
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 6616
ClinVar RCV Id: RCV000006995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334649.1:p.Met577Thr
CA253899
NM_001347720.2:c.1730T>C