Allele Registry

Canonical Allele Identifier: PA102965

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000012676

RCV000802420

RCV001273715

ClinVar Variation:

11901

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Cys56Arg	CA121763 NM_000128.4:c.166T>C