Allele Registry

Canonical Allele Identifier: PA658809642

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000649961

ClinVar Variation:

540039

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Arg1213Trp	CA7373328 NM_022489.4:c.3637C>T