Canonical Allele Identifier: PA2580345306
Gene: B4GALT7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715993
ClinVar RCV Id: RCV002295784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009186.1:p.Arg62Ser
CA362373067
NM_007255.3:c.186G>T
CA362373068
NM_007255.3:c.186G>C