Canonical Allele Identifier: PA354666
Gene: VCX3A HGNC NCBI

Linked Data

ClinVar Variation Id: 218736
ClinVar RCV Id: RCV000202930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057463.2:p.Val140Met
CA249129
NM_016379.4:c.418G>A