Canonical Allele Identifier: PA645490244
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312711
ClinVar RCV Id: RCV000370054 RCV000508357 RCV000649975 RCV001697662 RCV002450862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Ser1188Phe
CA7373307
NM_022489.4:c.3563C>T