Canonical Allele Identifier: PA2830156830
Gene: COLQ HGNC NCBI

Linked Data

ClinVar Variation Id: 2688854
ClinVar RCV Id: RCV003486047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_536800.2:p.Gly194Val
CA70613055
NM_080539.4:c.581G>T