Canonical Allele Identifier: PA174534
Gene: COPS6 HGNC NCBI

Linked Data

ClinVar Variation Id: 161652
ClinVar RCV Id: RCV000149188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006824.2:p.Ser211Arg
CA174533
NM_006833.5:c.631A>C
CA368433970
NM_006833.5:c.633T>A
CA368433972
NM_006833.5:c.633T>G