Allele Registry

Canonical Allele Identifier: PA658825430

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000665214

RCV002530648

ClinVar Variation:

550462

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Arg326His	CA358938142 NM_000128.4:c.977G>A