Canonical Allele Identifier: PA645438907
Gene: B3GALT6 HGNC NCBI

Linked Data

ClinVar Variation Id: 283597
ClinVar RCV Id: RCV000360273 RCV003165730 RCV001332792 RCV001503677
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542172.2:p.Asp285Asn
CA513450
NM_080605.3:c.853G>A