Allele Registry

Canonical Allele Identifier: PA102871

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000012673

ClinVar Variation:

11898

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Arg326Cys	CA121757 NM_000128.4:c.976C>T