Allele Registry

Canonical Allele Identifier: PA118378

Gene: B3GALNT1 HGNC NCBI

ClinVar Allele:

21674

ClinVar RCV:

RCV000007014

ClinVar Variation:

6635

HGVS (amino-acid)	Matching Registered Transcripts
NP_003772.1:p.Gly271Arg	CA118377 NM_003781.4:c.811G>A CA355255070 NM_003781.4:c.811G>C