Canonical Allele Identifier: PA2580345310
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202208
ClinVar RCV Id: RCV002647878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Glu86Gln
CA3586421
NM_007255.3:c.256G>C