Canonical Allele Identifier: PA645421422
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Arg806Cys
CA3750918
NM_080680.3:c.2416C>T