Allele Registry

Canonical Allele Identifier: PA097381

Gene: F2 HGNC NCBI

ClinVar Allele:

28341

ClinVar RCV:

RCV000014229

RCV000994617

RCV001108917

RCV001108918

RCV001794445

ClinVar Variation:

13302

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Glu200Lys	CA090909 NM_000506.5:c.598G>A