Allele Registry

Canonical Allele Identifier: PA103190

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000059019

RCV000454166

ClinVar Variation:

68187

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Ser575Leu	CA219128 NM_000128.4:c.1724C>T