Canonical Allele Identifier: PA182106
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Arg1667His
CA182105
NM_080680.3:c.5000G>A