ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826946931
Gene: F9
HGNC
NCBI
Linked Data
ClinVar Variation Id:
10593
ClinVar RCV Id:
RCV000011339
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001300842.1:p.Val190Phe
CA255355
NM_001313913.2:c.568G>T