Canonical Allele Identifier: PA2825051377
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 3233615
ClinVar RCV Id: RCV004526465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Lys446Gln
CA414447411
NM_000133.4:c.1336A>C