Canonical Allele Identifier: PA2580105444
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2184672
ClinVar RCV Id: RCV002632292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Val195Gly
CA336137420
NM_000133.4:c.584T>G