Canonical Allele Identifier: PA2580505117
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721912
ClinVar RCV Id: RCV002302260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569711.2:p.Pro692Leu
CA10065951
NM_130444.2:c.2075C>T