Canonical Allele Identifier: PA2825351079
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245865
ClinVar RCV Id: RCV000235504 RCV001243475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Glu395Lys
CA7372522
NM_001031714.3:c.1183G>A