ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826947027
Gene: F9
HGNC
NCBI
Linked Data
ClinVar Variation Id:
626950
ClinVar RCV Id:
RCV000851629
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001300842.1:p.Ala299Thr
CA414445354
NM_001313913.2:c.895G>A