Allele Registry

Canonical Allele Identifier: PA2830129518

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV001979191

ClinVar Variation:

1464700

HGVS (amino-acid)	Matching Registered Transcripts
NP_542410.2:p.Gly701Ala	CA363644128 NM_080679.3:c.2102G>C