Canonical Allele Identifier: PA2825350343
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_001026884.3:p.Ala28Val
CA391224777
NM_001031714.3:c.83C>T