Allele Registry

Canonical Allele Identifier: PA103044

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000012678

ClinVar Variation:

11903

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Gly418Val	CA121767 NM_000128.4:c.1253G>T