Canonical Allele Identifier: PA2825351874
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439827
ClinVar RCV Id: RCV001113917 RCV000649981 RCV001810994 RCV002438233 RCV003419879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Lys962Thr
CA7373121
NM_001031714.3:c.2885A>C