Allele Registry

Canonical Allele Identifier: PA103107

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000012677

RCV000059034

ClinVar Variation:

11902

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Lys270Ile	CA121765 NM_000128.4:c.809A>T