Allele Registry

Canonical Allele Identifier: PA2830129694

Gene: COL11A2 HGNC NCBI

ClinVar Allele:

307208

ClinVar RCV:

RCV000290480

RCV000344614

RCV000379273

RCV000400234

RCV001538789

ClinVar Variation:

356398

HGVS (amino-acid)	Matching Registered Transcripts
NP_542410.2:p.Gly788Ala	CA3750764 NM_080679.3:c.2363G>C