Allele Registry

Canonical Allele Identifier: PA281696

Gene: COL11A1 HGNC NCBI

ClinVar RCV:

RCV000018669

ClinVar Variation:

17131

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177638.1:p.Gly586Val	CA281694 NM_001190709.2:c.1757G>T