Canonical Allele Identifier: PA2829703974
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3132722
ClinVar RCV Id: RCV004423632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Ser89Phe
CA3586425
NM_007255.3:c.266C>T