Canonical Allele Identifier: PA2499275999
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1208774
ClinVar RCV Id: RCV001577210 RCV001866070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Ile271Leu
CA132896883
NM_007255.3:c.811A>C