Canonical Allele Identifier: PA916072122
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 599128
ClinVar RCV Id: RCV000735726 RCV000790332 RCV001535996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Glu184Lys
CA391213247
NM_032714.3:c.550G>A