Canonical Allele Identifier: PA109253
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 216926
ClinVar RCV Id: RCV000197147 RCV000851896 RCV000851897 RCV001378167 RCV001781582
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Ala279Thr
CA277507
NM_000133.4:c.835G>A