Canonical Allele Identifier: PA2830167878
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099420
ClinVar RCV Id: RCV003022988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569711.2:p.Pro1361Ala
CA410499296
NM_130444.2:c.4081C>G