Allele Registry

Canonical Allele Identifier: PA2830131037

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV002811356

ClinVar Variation:

2003674

HGVS (amino-acid)	Matching Registered Transcripts
NP_542411.2:p.Ala37Thr	CA363613446 NM_080680.3:c.109G>A