ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826947062
Gene: F9
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000011385
RCV001001418
ClinVar Variation:
10639
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001300842.1:p.Val336Phe
CA255427
NM_001313913.2:c.1006G>T