Allele Registry

Canonical Allele Identifier: PA916058740

Gene: COL18A1 HGNC NCBI

ClinVar RCV:

RCV000489683

ClinVar Variation:

427063

HGVS (amino-acid)	Matching Registered Transcripts
NP_569711.2:p.Gly1695Trp	CA410502175 NM_130444.2:c.5083G>T