Canonical Allele Identifier: PA2580415569
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2490751
ClinVar RCV Id: RCV004278048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059132.1:p.Ala272Asp
CA10270206
NM_017436.7:c.815C>A