Allele Registry

Canonical Allele Identifier: PA2830130556

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000415302

ClinVar Variation:

374129

HGVS (amino-acid)	Matching Registered Transcripts
NP_542410.2:p.Gly1370Val	CA3750080 NM_080679.3:c.4109G>T