Canonical Allele Identifier: PA103927
Gene: COCH HGNC NCBI

Linked Data

ClinVar Variation Id: 6611
ClinVar RCV Id: RCV000006990 RCV000211754 RCV000844626 RCV001093033 RCV001375055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128530.1:p.Pro51Ser
CA253889
NM_001135058.2:c.151C>T