Canonical Allele Identifier: PA2825351987
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472850
ClinVar RCV Id: RCV000549964 RCV001328082 RCV002324037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Arg1045Trp
CA7373186
NM_001031714.3:c.3133C>T