Canonical Allele Identifier: PA2828833855
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1959477
ClinVar RCV Id: RCV002701296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366429.1:p.Pro1001Leu
CA10067601
NM_001379500.1:c.3002C>T