Canonical Allele Identifier: PA2573252046
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482069
ClinVar RCV Id: RCV001994406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Arg121Thr
CA3586451
NM_007255.3:c.362G>C