Canonical Allele Identifier: PA2829703960
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3132720
ClinVar RCV Id: RCV004423630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Ala37Thr
CA362372638
NM_007255.3:c.109G>A