Allele Registry

Canonical Allele Identifier: PA2830160090

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV001894920

ClinVar Variation:

1369527

HGVS (amino-acid)	Matching Registered Transcripts
NP_542412.2:p.Gln1535Arg	CA363617367 NM_080681.3:c.4604A>G