Canonical Allele Identifier: PA1139725603
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 849803
ClinVar RCV Id: RCV001053837 RCV001538738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Arg125Gln
CA3586454
NM_007255.3:c.374G>A