Canonical Allele Identifier: PA2825351279
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 518072
ClinVar RCV Id: RCV001112479 RCV001698446 RCV001446526 RCV003945559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Ser483Phe
CA7372571
NM_001031714.3:c.1448C>T