Allele Registry

Canonical Allele Identifier: PA111355

Gene: INF2 HGNC NCBI

ClinVar Allele:

39822

ClinVar RCV:

RCV000023850

ClinVar Variation:

30865

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Cys104Phe	CA129510 NM_022489.4:c.311G>T