Allele Registry

Canonical Allele Identifier: PA658809620

Gene: INF2 HGNC NCBI

ClinVar RCV:

RCV000649959

RCV002442343

ClinVar Variation:

540037

HGVS (amino-acid)	Matching Registered Transcripts
NP_071934.3:p.Ala1020Val	CA7373169 NM_022489.4:c.3059C>T