Canonical Allele Identifier: PA2499295781
Gene: B3GALT6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1204929
ClinVar RCV Id: RCV001882678 RCV001571427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542172.2:p.Trp91Cys
CA16755168
NM_080605.3:c.273G>C
CA337823914
NM_080605.3:c.273G>T