Canonical Allele Identifier: PA2825351088
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373658
ClinVar RCV Id: RCV000414390 RCV001226432 RCV002338975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Val397Met
CA7372524
NM_001031714.3:c.1189G>A