Canonical Allele Identifier: PA2825966668
Gene: VCAN HGNC NCBI
ClinVar RCV:
RCV002048922
ClinVar Variation:
1523497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157569.1:p.Asn2242Ser
CA3334068
NM_001164097.1:c.6725A>G