Allele Registry

Canonical Allele Identifier: PA2825048832

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV004385778

ClinVar Variation:

3091392

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Ser293Ala	CA3163814 NM_000128.4:c.877T>G