Canonical Allele Identifier: PA2826976870
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2351276
ClinVar RCV Id: RCV004194400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Val207Gly
CA10270255
NM_001318038.3:c.620T>G