Allele Registry

Canonical Allele Identifier: PA103137

Gene: F11 HGNC NCBI

ClinVar Allele:

26934

ClinVar RCV:

RCV000012670

ClinVar Variation:

11895

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Phe460Val	CA121750 NM_000128.4:c.1378T>G