Allele Registry

Canonical Allele Identifier: PA103003

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000059020

RCV000671144

ClinVar Variation:

68188

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Glu597Lys	CA219130 NM_000128.4:c.1789G>A