Canonical Allele Identifier: PA109901
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10579
ClinVar RCV Id: RCV000011325 RCV000795416 RCV001810846 RCV002247325 RCV002496325 RCV003430636
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Gly106Ser
CA255329
NM_000133.4:c.316G>A