Canonical Allele Identifier: PA111355
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30865
ClinVar RCV Id: RCV000023850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Cys104Phe
CA129510
NM_022489.4:c.311G>T