Canonical Allele Identifier: PA658805334
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 517184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Leu1642Val
CA3749954
NM_080680.3:c.4924C>G