Canonical Allele Identifier: PA2826946947
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 627124
ClinVar RCV Id: RCV000851863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Lys209Thr
CA414443111
NM_001313913.2:c.626A>C