Canonical Allele Identifier: PA111394
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 523533
ClinVar RCV Id: RCV000626959 RCV000711995 RCV000790334 RCV000735784 RCV001860480 RCV002468593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Glu220Lys
CA391213465
NM_022489.4:c.658G>A