Allele Registry

Canonical Allele Identifier: PA096572

Gene: B4GALNT1 HGNC NCBI

ClinVar Allele:

75110

ClinVar RCV:

RCV000054423

ClinVar Variation:

60527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001469.1:p.Asp433Ala	CA10575595 NM_001478.5:c.1298A>C