Canonical Allele Identifier: PA916058737
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 340273
ClinVar RCV Id: RCV000262928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569711.2:p.Asp1675Asn
CA10653683
NM_130444.2:c.5023G>A