Canonical Allele Identifier: PA2825351596
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540057
ClinVar RCV Id: RCV000649983
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Glu719Lys
CA7372850
NM_001031714.3:c.2155G>A