Canonical Allele Identifier: PA109966
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 627130
ClinVar RCV Id: RCV000851869
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Gly253Arg
CA414443212
NM_000133.4:c.757G>A
CA414443215
NM_000133.4:c.757G>C