Canonical Allele Identifier: PA2825352053
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245863
ClinVar RCV Id: RCV000398507 RCV000553031 RCV001171335 RCV001705305 RCV002321901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Arg1074Lys
CA7373206
NM_001031714.3:c.3221G>A