Allele Registry

Canonical Allele Identifier: PA3057264334

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV004623055

ClinVar Variation:

3276924

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Val218Ile	CA358959140 NM_000128.4:c.652G>A