Canonical Allele Identifier: PA096549
Gene: B3GALT6 HGNC NCBI

Linked Data

ClinVar Variation Id: 60488
ClinVar RCV Id: RCV000054394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542172.2:p.Ser65Gly
CA144526
NM_080605.3:c.193A>G