Canonical Allele Identifier: PA2830156839
Gene: COLQ HGNC NCBI

Linked Data

ClinVar Variation Id: 1046437
ClinVar RCV Id: RCV001350996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_536800.2:p.Arg202Gln
CA2276018
NM_080539.4:c.605G>A