ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA105239
Gene: F8
HGNC
NCBI
Linked Data
ClinVar Variation Id:
10225
ClinVar RCV Id:
RCV000010938
RCV003656622
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000123.1:p.Arg550His
CA255115
NM_000132.4:c.1649G>A