Canonical Allele Identifier: PA109297
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10585
ClinVar RCV Id: RCV000011331 RCV000851602 RCV001390296 RCV002284168 RCV002247326
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Arg191His
CA255342
NM_000133.4:c.572G>A