Canonical Allele Identifier: PA2826947020
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV000011351
ClinVar Variation:
10605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Pro295Leu
CA255375
NM_001313913.2:c.884C>T