Canonical Allele Identifier: PA2828691273
Gene: GBF1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364070.1:p.His591Asp
CA5663349
NM_001377141.1:c.1771C>G