Canonical Allele Identifier: PA2830130866
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2115442
ClinVar RCV Id: RCV003032663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Cys1548Gly
CA363616216
NM_080679.3:c.4642T>G