Canonical Allele Identifier: PA2826976847
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 1483587
ClinVar RCV Id: RCV002025470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Met114Leu
CA411812539
NM_001318038.3:c.340A>T
CA411812541
NM_001318038.3:c.340A>C
CA2573158195
NM_001318038.3:c.339_340delinsTT