Allele Registry

Canonical Allele Identifier: PA916039423

Gene: F11 HGNC NCBI

ClinVar Allele:

26940

ClinVar RCV:

RCV000012676

RCV000802420

RCV001273715

ClinVar Variation:

11901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341733.1:p.Cys56Arg	CA121763 NM_001354804.2:c.166T>C