Allele Registry

Canonical Allele Identifier: PA645421505

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000415302

ClinVar Variation:

374129

HGVS (amino-acid)	Matching Registered Transcripts
NP_542411.2:p.Gly1477Val	CA3750080 NM_080680.3:c.4430G>T