Allele Registry

Canonical Allele Identifier: PA645294914

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000428449

RCV000851667

RCV001273723

ClinVar Variation:

381729

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Pro400Leu	CA3163918 NM_000128.4:c.1199C>T