Canonical Allele Identifier: PA2830131374
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2756983
ClinVar RCV Id: RCV003567036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Arg1616Lys
CA363617434
NM_080680.3:c.4847G>A