Canonical Allele Identifier: PA2573203943
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 1507984
ClinVar RCV Id: RCV002040300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334649.1:p.Ala578Pro
CA389349556
NM_001347720.2:c.1732G>C