Canonical Allele Identifier: PA2573269578
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 1438947
ClinVar RCV Id: RCV001974824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059132.1:p.Thr210Pro
CA10270252
NM_017436.7:c.628A>C