Allele Registry

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Canonical Allele Identifier: PA915991052

Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 647607

ClinVar RCV Id: RCV000802152 RCV001549773

ClinVar Variation Id: 3132721

ClinVar RCV Id: RCV004423631

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_009186.1:p.Arg73His	CA3586408 NM_007255.3:c.218G>A CA915942738 NM_007255.3:c.218_219delinsAC