Allele Registry

Canonical Allele Identifier: PA117649

Gene: B4GALT7 HGNC NCBI

ClinVar RCV:

RCV000005965

RCV000258718

RCV000413846

RCV000779599

RCV002482832

ClinVar Variation:

5613

HGVS (amino-acid)	Matching Registered Transcripts
NP_009186.1:p.Arg270Cys	CA117648 NM_007255.3:c.808C>T