Canonical Allele Identifier: PA916058611
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 340200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569711.2:p.Val646Met
CA10065850
NM_130444.2:c.1936G>A