Canonical Allele Identifier: PA2829190069
Gene: GBF1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001378857.1:p.Glu519Gln
CA5663295
NM_001391928.1:c.1555G>C