Canonical Allele Identifier: PA2573214853
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494841
ClinVar RCV Id: RCV001989620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366429.1:p.Pro956Ser
CA410499355
NM_001379500.1:c.2866C>T