Canonical Allele Identifier: PA2830004332
Gene: INF2 HGNC NCBI
ClinVar RCV:
RCV003031800
ClinVar Variation:
2109247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Ala28Val
CA391224777
NM_022489.4:c.83C>T