Canonical Allele Identifier: PA916021250
Gene: F9 HGNC NCBI
ClinVar Allele:
649734
ClinVar RCV:
RCV000806960
ClinVar Variation:
651569
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Val30Ile
CA414434500
NM_001313913.2:c.88G>A