Allele Registry

Canonical Allele Identifier: PA2830159963

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000415302

ClinVar Variation:

374129

HGVS (amino-acid)	Matching Registered Transcripts
NP_542412.2:p.Gly1391Val	CA3750080 NM_080681.3:c.4172G>T