Canonical Allele Identifier: PA645421394
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Gly685Ala
CA10626490
NM_080680.3:c.2054G>C