Canonical Allele Identifier: PA2825351864
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540052
ClinVar RCV Id: RCV000649977 RCV001771896
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Arg953Gln
CA391222788
NM_001031714.3:c.2858G>A