Canonical Allele Identifier: PA2825351803
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540045
ClinVar RCV Id: RCV000649967 RCV002440354 RCV003420140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Leu919Val
CA7373055
NM_001031714.3:c.2755C>G