Canonical Allele Identifier: PA255380
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10606
ClinVar RCV Id: RCV000011352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Ala337Pro
CA255378
NM_000133.4:c.1009G>C