Canonical Allele Identifier: PA2580235578
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2066695
ClinVar RCV Id: RCV002966207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366429.1:p.Lys909Asn
CA410499079
NM_001379500.1:c.2727G>C
CA410499080
NM_001379500.1:c.2727G>T