Canonical Allele Identifier: PA915987900
Gene: VCAN HGNC NCBI

Linked Data

ClinVar Variation Id: 167821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157569.1:p.Glu548Gly
CA180480
NM_001164097.1:c.1643A>G