Allele Registry

Canonical Allele Identifier: PA2830159212

Gene: COL11A2 HGNC NCBI

ClinVar RCV:

RCV002122169

ClinVar Variation:

1592134

HGVS (amino-acid)	Matching Registered Transcripts
NP_542412.2:p.Ser745Leu	CA3750872 NM_080681.3:c.2234C>T