Canonical Allele Identifier: PA110391
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10650
ClinVar RCV Id: RCV000011396 RCV002512972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Ser411Gly
CA255441
NM_000133.4:c.1231A>G
CA2695236388
NM_000133.4:c.1230_1231delinsCG