Allele Registry

Canonical Allele Identifier: PA103235

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000012672

ClinVar Variation:

11897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Thr404Asn	CA121755 NM_000128.4:c.1211C>A