Canonical Allele Identifier: PA2829190060
Gene: GBF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3098864
ClinVar RCV Id: RCV004395229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001378857.1:p.Ser297Phe
CA212180962
NM_001391928.1:c.890C>T