Canonical Allele Identifier: PA2830004389
Gene: INF2 HGNC NCBI
ClinVar RCV:
RCV002008879
ClinVar Variation:
1487843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Gly63Asp
CA267330439
NM_022489.4:c.188G>A