Canonical Allele Identifier: PA2826161174
Gene: COL11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291548
ClinVar Variation Id: 547199
ClinVar RCV Id: RCV000659306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177638.1:p.Gly110Arg
CA975481
NM_001190709.2:c.328G>C
CA341167975
NM_001190709.2:c.328G>A