Canonical Allele Identifier: PA2826976890
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2171164
ClinVar RCV Id: RCV003088793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Pro305Leu
CA10270185
NM_001318038.3:c.914C>T