Canonical Allele Identifier: PA2829539752
Gene: VCAN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004376.2:p.Asn3229Ser
CA3334068
NM_004385.5:c.9686A>G