Canonical Allele Identifier: PA916021259
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV001001440
ClinVar Variation:
811523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Cys64Arg
CA336130710
NM_001313913.2:c.190T>C