Canonical Allele Identifier: PA2573076494
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 447120
ClinVar Variation Id: 447121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366429.1:p.Gly928Arg
CA10067464
NM_001379500.1:c.2782G>C
CA10067465
NM_001379500.1:c.2782G>A