Canonical Allele Identifier: PA110001
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10611
ClinVar RCV Id: RCV000011357 RCV000851648
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Gly357Arg
CA255389
NM_000133.4:c.1069G>A
CA414445690
NM_000133.4:c.1069G>C