Canonical Allele Identifier: PA2580484918
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2109247
ClinVar RCV Id: RCV003031800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Ala28Val
CA391224777
NM_032714.3:c.83C>T