Canonical Allele Identifier: PA2826946909
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10588
ClinVar RCV Id: RCV000011334 RCV000244191 RCV000396693 RCV001521358 RCV001701639 RCV001810847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Thr156Ala
CA121125
NM_001313913.2:c.466A>G