Canonical Allele Identifier: PA2825352191
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 426793
ClinVar RCV Id: RCV000490158 RCV000649970 RCV002455952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Thr1179Ala
CA7373296
NM_001031714.3:c.3535A>G