Canonical Allele Identifier: PA2826946971
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 216926
ClinVar RCV Id: RCV000197147 RCV000851896 RCV000851897 RCV001378167 RCV001781582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Ala241Thr
CA277507
NM_001313913.2:c.721G>A