Allele Registry

Canonical Allele Identifier: PA115692

Gene: A4GALT HGNC NCBI

ClinVar RCV:

RCV000002815

ClinVar Variation:

2696

HGVS (amino-acid)	Matching Registered Transcripts
NP_059132.1:p.Phe81del	CA115691 NM_017436.7:c.241_243del