Canonical Allele Identifier: PA2826947088
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV003050660
ClinVar Variation:
2138745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Cys358Tyr
CA414446367
NM_001313913.2:c.1073G>A