Canonical Allele Identifier: PA096572
Gene: B4GALNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 60527
ClinVar RCV Id: RCV000054423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001469.1:p.Asp433Ala
CA10575595
NM_001478.5:c.1298A>C