Allele Registry

Canonical Allele Identifier: PA2830159498

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000437358

RCV000764646

ClinVar Variation:

391897

HGVS (amino-acid)	Matching Registered Transcripts
NP_542412.2:p.Thr1011Pro	CA3750574 NM_080681.3:c.3031A>C