Canonical Allele Identifier: PA2573252032
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1676000
ClinVar RCV Id: RCV002214369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Phe105Leu
CA362373826
NM_007255.3:c.313T>C
CA362373838
NM_007255.3:c.315C>A
CA362373839
NM_007255.3:c.315C>G