Canonical Allele Identifier: PA2742006672
Gene: COL18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2819117
ClinVar RCV Id: RCV003706148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569711.2:p.Phe33Leu
CA410505123
NM_130444.2:c.97T>C
CA410505128
NM_130444.2:c.99C>A
CA410505129
NM_130444.2:c.99C>G