Canonical Allele Identifier: PA2580415563
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2138456
ClinVar RCV Id: RCV003064661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059132.1:p.Ala219Val
CA10270247
NM_017436.7:c.656C>T