Allele Registry

Canonical Allele Identifier: PA2499228660

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV001479237

RCV001832626

ClinVar Variation:

1141692

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Ser419Thr	CA3163936 NM_000128.4:c.1255T>A