Canonical Allele Identifier: PA916058735
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 340270
ClinVar RCV Id: RCV000260062 RCV001861184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569711.2:p.Val1640Ile
CA10068005
NM_130444.2:c.4918G>A