Allele Registry

Canonical Allele Identifier: PA916072015

Gene: INF2 HGNC NCBI

ClinVar Allele:

39822

ClinVar RCV:

RCV000023850

ClinVar Variation:

30865

HGVS (amino-acid)	Matching Registered Transcripts
NP_116103.1:p.Cys104Phe	CA129510 NM_032714.3:c.311G>T