Allele Registry

Canonical Allele Identifier: PA3057243213

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV000018659

ClinVar Variation:

17122

HGVS (amino-acid)	Matching Registered Transcripts
NP_542412.2:p.Glu855_Pro864delinsAla	CA281688 NM_080681.3:c.2564_2590del