Canonical Allele Identifier: PA2828833225
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1467878
ClinVar RCV Id: RCV001968717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366429.1:p.Thr282Ala
CA410514383
NM_001379500.1:c.844A>G