Allele Registry

Canonical Allele Identifier: PA110120

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000851938

ClinVar Variation:

627177

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Ile136Thr	CA414438824 NM_000133.4:c.407T>C