Canonical Allele Identifier: PA2499271668
Gene: COLQ HGNC NCBI

Linked Data

ClinVar Variation Id: 1002338
ClinVar RCV Id: RCV001298753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005668.2:p.Pro221Ser
CA351598080
NM_005677.4:c.661C>T