Canonical Allele Identifier: PA111404
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30867
ClinVar RCV Id: RCV000023852 RCV000235466 RCV001378421 RCV002362594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Leu128Pro
CA129512
NM_022489.4:c.383T>C