Canonical Allele Identifier: PA1139700974
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 882738
ClinVar RCV Id: RCV001112669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004077.1:p.Pro89His
CA7142986
NM_004086.3:c.266C>A