Canonical Allele Identifier: PA2825351513
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540042
ClinVar RCV Id: RCV000649964 RCV002422390 RCV002261158 RCV002294363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Glu653Lys
CA7372766
NM_001031714.3:c.1957G>A