Allele Registry

Canonical Allele Identifier: PA2826556724

Gene: B4GALNT1 HGNC NCBI

ClinVar Allele:

75110

ClinVar RCV:

RCV000054423

ClinVar Variation:

60527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263397.1:p.Asp378Ala	CA10575595 NM_001276468.2:c.1133A>C