Canonical Allele Identifier: PA2573214829
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1437175
ClinVar RCV Id: RCV001933929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366429.1:p.Ala918Thr
CA10067446
NM_001379500.1:c.2752G>A