Canonical Allele Identifier: PA2830128831
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542410.2:p.Pro296Leu
CA3751427
NM_080679.3:c.887C>T