Canonical Allele Identifier: PA645421777
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 389383
ClinVar RCV Id: RCV000429366 RCV001066223 RCV002522511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Ala272Thr
CA3586692
NM_007255.3:c.814G>A