Canonical Allele Identifier: PA2825967517
Gene: VCAN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157570.1:p.Asn1475Ser
CA3334068
NM_001164098.1:c.4424A>G