Allele Registry

Canonical Allele Identifier: PA645294916

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000383804

RCV000851679

ClinVar Variation:

291081

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Ala430Thr	CA3163944 NM_000128.4:c.1288G>A