Canonical Allele Identifier: PA2580105534
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV003050660
ClinVar Variation:
2138745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Cys396Tyr
CA414446367
NM_000133.4:c.1187G>A