Allele Registry

Canonical Allele Identifier: PA2830130786

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV001894920

ClinVar Variation:

1369527

HGVS (amino-acid)	Matching Registered Transcripts
NP_542410.2:p.Gln1514Arg	CA363617367 NM_080679.3:c.4541A>G