Canonical Allele Identifier: PA2573251995
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423842
ClinVar RCV Id: RCV003891318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Ser30Phe
CA362372522
NM_007255.3:c.89C>T