Canonical Allele Identifier: PA2825351282
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312688
ClinVar RCV Id: RCV000267568 RCV000419174 RCV000860568 RCV001727680 RCV002392855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Cys484Tyr
CA7372572
NM_001031714.3:c.1451G>A