Canonical Allele Identifier: PA255328
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10578
ClinVar RCV Id: RCV000011324 RCV001810845 RCV003764550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Pro101Ala
CA255326
NM_000133.4:c.301C>G