Allele Registry

Canonical Allele Identifier: PA645421463

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000437358

RCV000764646

ClinVar Variation:

391897

HGVS (amino-acid)	Matching Registered Transcripts
NP_542411.2:p.Thr1097Pro	CA3750574 NM_080680.3:c.3289A>C