Canonical Allele Identifier: PA2825351476
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 498799
ClinVar RCV Id: RCV000597249 RCV001086165 RCV002413674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Arg622Gly
CA7372691
NM_001031714.3:c.1864C>G