Allele Registry

Canonical Allele Identifier: PA281697

Gene: COL11A1 HGNC NCBI

ClinVar RCV:

RCV000018669

ClinVar Variation:

17131

HGVS (amino-acid)	Matching Registered Transcripts
NP_542196.2:p.Gly637Val	CA281694 NM_080629.3:c.1910G>T