Canonical Allele Identifier: PA2829190319
Gene: GBF1 HGNC NCBI
ClinVar RCV:
RCV004395229
ClinVar Variation:
3098864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001378860.1:p.Ser297Phe
CA212180962
NM_001391931.1:c.890C>T