Canonical Allele Identifier: PA2830156609
Gene: COLQ HGNC NCBI

Linked Data

ClinVar Variation Id: 1363279
ClinVar RCV Id: RCV001902171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_536799.1:p.Gly209Ser
CA351598108
NM_080538.2:c.625G>A