Allele Registry

Canonical Allele Identifier: PA102821

Gene: F11 HGNC NCBI

ClinVar Allele:

26938

ClinVar RCV:

RCV000012674

ClinVar Variation:

11899

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Ala430Val	CA121759 NM_000128.4:c.1289C>T