Allele Registry

Canonical Allele Identifier: PA2830167822

Gene: COL18A1 HGNC NCBI

ClinVar RCV:

RCV001995029

ClinVar Variation:

1469729

HGVS (amino-acid)	Matching Registered Transcripts
NP_569711.2:p.Gly1325Trp	CA410499093 NM_130444.2:c.3973G>T