Canonical Allele Identifier: PA2825351692
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540036
ClinVar RCV Id: RCV000786890 RCV000649958 RCV002458127 RCV002461961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Asp814Asn
CA7372939
NM_001031714.3:c.2440G>A