Canonical Allele Identifier: PA2830167816
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519663
ClinVar RCV Id: RCV002043756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569711.2:p.Ala1321Gly
CA410499055
NM_130444.2:c.3962C>G