Canonical Allele Identifier: PA916056703
Gene: B3GALT6 HGNC NCBI

Linked Data

ClinVar Variation Id: 661179
ClinVar RCV Id: RCV000818547 RCV001093298 RCV002537434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542172.2:p.Ala114Glu
CA513317
NM_080605.3:c.341C>A