Canonical Allele Identifier: PA2827198738
Gene: AFG2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1275863
ClinVar RCV Id: RCV003442896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310569.1:p.Phe360Ser
CA392264566
NM_001323640.2:c.1079T>C